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<h3>Job Description</h3>
Job Description
Description Introduction
Paragonix Technologies markets organ transportation devices that safeguard organs during the journey between donor and recipient patients. Our devices incorporate clinically proven and medically trusted hypothermic preservation techniques in a novel suspension system to provide unprecedented physical and thermal protection. Our product portfolio spans cardiac, thoracic, and abdominal preservation devices to improve donor organ quality and extend donor organ transport time. Paragonix also markets transplant procurement services to the transplant community.
As Clinical Research Statistician you will be responsible for the design, validation, analysis and interpretation of clinical data from multiple registries in support of product development and business objectives. The position is based out of our Waltham office in the greater Boston area. There is an option to work in a hybrid environment, at least 3 days in-office is expected.
Position Responsibilities
<ul>
<li>Use advanced statistical methods to validate and analyze data</li>
<li>Write efficient code for processing data utilizing R statistical software.</li>
<li>Create processes for validating quality and accuracy of data.</li>
<li>Perform statistical programming and data analysis, as well as database cleaning, verification and validation, and quality review of statistical analyses</li>
<li>Manage resources, timelines and priorities for assigned projects</li>
<li>Work with clinical affairs staff and clinical investigators to determine appropriate study and protocol design</li>
<li>Provide statistical expertise to clinical affairs staff to ensure that the CRFs and database meet the study design needs</li>
<li>Responsible for statistical analysis plans (SAP) and development of tables/listings/figures for statistical reports</li>
<li>Prepare statistical methods and results sections for presentations, reports, and peer-reviewed manuscripts</li>
<li>Participate in preparing and writing statistical content for 501k and other FDA required reports</li>
<li>May be involved in analyses of 'big data' for market assessments, as well as from public sources (such as UNOS)</li>
<li>Organized, self-starter; ability to work in a fast-paced environment with a "roll up your sleeves" attitude</li>
<li>Ability to work independently and as part of a team</li>
<li>Excellent oral and written communication, and interpersonal skills necessary to interact with a wide range of individuals and cross-functional stakeholders.</li>
</ul>
Experience
<ul>
<li>At least 2-4 years of statistical work experience in a biomedical life science or medical device company, including programming using SAS or R statistical software.</li>
<li>Comprehensive knowledge of statistical methods</li>
<li>Prior healthcare or medical device industry experience</li>
<li>Proficiency in R programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming languages such as SAS, Python etc. is a plus.</li>
<li>Prior experience working with research and/or healthcare data.</li>
</ul>
Education
<ul>
<li>Bachelor's degree in biostatistics, statistics, epidemiology or similar area of study, required.</li>
<li>Master's degree or higher in biostatistics or relevant area of study preferred.</li>
<li>Proficient in Microsoft Office Suite.</li>
<li>Transplant surgery /medical knowledge is a plus.</li>
<li>Experience or knowledge of FDA regulations or submissions is a plus.</li>
</ul>
Salary range is $73,000 to $85,000 depending on experience.
Description Conclusion

Clinical Research Statistician

<h3>Job Description</h3>
Job DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute aiming to &nbsp;catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians.&nbsp;Why?&nbsp;Protein dysfunctions directly cause many diseases, such as Alzheimer’s disease. Yet, proteins remain understudied because of technological hurdles.&nbsp;How? To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org.&nbsp;PTI’s new approach requires synergy between a diverse team of chemists, machine learning engineers, biologists, and mass spectrometrists. Alzheimer’s disease and aging will be among the first focuses of this technology-driven research organization.&nbsp;New career opportunitiesMembers of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals.&nbsp;&nbsp;Summary of PositionWe are looking for an experienced Mass Spectrometrist who will be working on maintaining MS instruments for running multitudes of samples for a variety of projects in addition to other responsibilities such as advancing and executing hypothesis-driven experiments.&nbsp;In order to be seriously considered for this position, we require a cover letter as part of the candidate’s application.Responsibilities
<ul>
<li>You will setup, operate, and maintain (i.e. vent and clean) mass spectrometers from multiple major vendors (Thermo, Bruker, Sciex, etc.).</li>
<li>Analyze experimental data and interpret results for internal and public presentation.</li>
<li>Training team members to use instruments independently.</li>
<li>Designing relevant proteomic experiments.</li>
<li>Perform protein sample preparation.</li>
<li>Preparation of lab reagents and media.</li>
<li>Inventory management and preparation reagents and samples.</li>
<li>Communication with purchasing and may be responsible for negotiating with various vendors.</li>
<li>May manage MTAs, software licenses, service contracts, and other documentation.</li>
</ul>
Required Qualifications
<ul>
<li>Masters or PhD in Biology, Biochemistry, or Chemistry.</li>
<li>5+ years of experience maintaining mass spectrometers.</li>
<li>Demonstrated experience optimizing LC-MS/MS methods for bottom-up proteomics (e.g. DDA/DIA/prioritized approaches).</li>
<li>Demonstrated mastery of chemistry techniques or molecular &amp; cellular biology techniques.&nbsp;&nbsp;</li>
<li>Demonstrated enthusiasm &amp; interest in bioanalytical chemistry.</li>
<li>High level of initiative and flexibility, excellent communication and teamwork skills.</li>
<li>Attention to detail and good time management skills.</li>
</ul>
Preferred Qualifications
<ul>
<li>Experience with mass spectrometry technological development (hardware or software).</li>
<li>Proficiency with statistical and computational methods (e.g. coding in Python/R).</li>
</ul>
We Offer
<ul>
<li>An opportunity to change the world and work with some of the smartest and the most talented experts from different fields.</li>
<li>Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from.</li>
<li>Company-paid group life, AD&amp;D, long- and short-term disability insurance.</li>
<li>15 days PTO + 10 sick days per year.</li>
<li>18 company holidays + your birthday off.</li>
<li>$5,000 per year educational reimbursement.</li>
<li>Up to 16 weeks paid parental leave.</li>
<li>Industry competitive salary.</li>
</ul>
We aim to help fill a structural gap in today's R&amp;D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&amp;D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations.&nbsp;We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Mass Spectrometrist

<h3>Job Description</h3>
Job DescriptionJob Title: Research Associate Location: Marlborough, MA 01581 Duration: 6 Months+ (possibilities of Extension) Pay Range: $43 - $48/hr. on w2 Summary: We are seeking a highly motivated Research Associate to support the development of cell therapy products, with a primary focus on formulation development. The successful candidate will contribute to development work on drug product, such as formulation design, manufacturing process development, product characterization, and evaluation of administration method. This role involved hands-on laboratory work including cell culture, preparation of drug product, other wet lab experiments, data analysis, and documentation such as drafting protocols and reports. The Research Associate will work under the guidance of a Scientist II. Key Responsibilities:
<ul>
<li>Support formulation development for cell therapy products, including process optimization and product evaluation.</li>
<li>Conduct cell-based experiments in a laboratory setting under supervision.</li>
<li>Perform basic cell culture and aseptic techniques within a biosafety cabinet (BSC).</li>
<li>Assist with formulation, analytical, and manufacturing tasks involving non-cellular components as needed.</li>
<li>Contribute to the development and evaluation of administration procedures simutated at clinical settings.</li>
<li>Maintain accurate compliant experimental records in accordance with Good Documentation Practice.</li>
<li>Draft study protocols and reports with guidance.</li>
</ul>
 Qualifications: Required:
<ul>
<li>BS degree with 5+ years of laboratory experience or MS with 2 years.</li>
<li>Hands-on experience with aseptic tissue culture techniques in a BSC.</li>
<li>Solid understanding of cell biology and cell-based assays.</li>
<li>Strong attention to detail and organizational skills.</li>
<li>Ability to work independently and collaborative within a team.</li>
<li>Self-motivated and proactive in learning new skills.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to analyze experimental data and summarize findings clearly.</li>
<li>Flexibility to work variable hours as needed.</li>
<li>Knowledge and experience of CMC (Chemistry Manufacturing and Control) development.</li>
</ul>
 Preferred:
<ul>
<li>Prior experience working in a GMP-regulated environment is highly desirable.</li>
<li>Knowledge and hands-on experience in drug product development.</li>
<li>Familiarity with GMP standards, ICH guidelines, and global compendial regulations including USP, JP and EP.</li>
<li>Prior experience with flow cytometry and plate-based assays.</li>
<li>Familiarity with data analysis and visualization tools such as GraphPad Prism and JMP.</li>
<li>Flexibility to work on weekends as needed.</li>
</ul>
 #sczr2

Research Associate

<h3>Job Description</h3>
Job Description
Notes Short term labeling project utilizing a proprietary interface. Will require contingents to sign the attached additional NDA on their first day of assignment. &nbsp; Job description: Faculty member with course and curriculum development efforts, scholarly research and data collection efforts. Contribute to the faculty member's research in ways that typically include writing and editing, data and information gathering, designing qualitative and quantitative research. Gain understanding of the research subject matter. Plan and conduct interviews, surveys, and literature reviews. Synthesize findings, analyze and interpret results. Assisting with the creation of presentations, summaries and articles on research topics.
Company DescriptionDella Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations. 
<h3>Company Description</h3>
Della Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations.

Research Assistant - Short Term Assignment

<h3>Job Description</h3>
Job Description
Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities.
Job Responsibilities:
● Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus.
● Communicate and coordinate with other scientists on a project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks.
● Collect and record data. Prepare summaries of experimental procedures and results and present data in team meetings.
● Develop, perform, interpret, and troubleshoot a broad range of in vitro assays including immune cell profiling, cytokine profiling, functional assays using primary cells, as well as cytotoxicity/apoptosis assays using primary and/or cultured cells. 
● Innovate and expand our assay portfolio by identifying, evaluating, and implementing new assay technologies through literature research, academic collaborations, and adaptation from other groups within the company.
Requirements
● Bachelor’s or Master’s degree with 1-3 years of academic or industry research experience. Demonstrated experience in small animal handling and pharmacology is highly preferred. 
● Experience with small animal handling, drug administration, and blood and tissue collection is preferred.
● Experience in cell biology, biochemistry, and/or molecular biology, in particular assay development and execution, is required. This includes cell-based assays, tissue culture, biochemical assay technologies, and protein and RNA expression analysis. 
● Experience with cell culture and in vitro assays is desirable.
● Experience in primary immune cell-based assays is strongly preferred. 
● Experience in flow cytometry (FACS) analysis is preferred.
● Demonstrate ability for quality execution, attention to detail, and proficiency in multi-tasking in a fast-paced environment.
● Collaborative team player. Be flexible and prioritize tasks based on team and company goals. 
● Communicate effectively at all levels, within teams, with internal and external collaborators. 
● Strong organizational skills. Maintain research data and records with the highest integrity. 
● Ability to multitask in a fast-paced environment.
Benefits
<ul>
<li>Medical Insurance </li>
<li>Dental Insurance </li>
<li>Vision Insurance </li>
<li>Health Reimbursement Accounts </li>
<li>Life and AD&amp;D Insurance </li>
<li>Short &amp; Long Term Disability Insurance </li>
<li>401K with Company Match</li>
<li>Paid Time Off</li>
<li>Paid Sick Days &amp; Holidays </li>
</ul>
BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Pharmacology Research Associate

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting:
Principal Scientist, CMC Radiochemistry
Description:
We are seeking an experienced Scientist I/II, CMC Radiochemistry to join Mariana Oncology's CMC organization, advancing personalized medicine and radiopharmaceuticals. You will be responsible for radiochemistry development through validations of pipeline projects leading to and enabling production, development, and advancement of radiotherapeutics and nuclear imaging probes. You will join the development efforts in support of the next generation radiotherapeutics for Mariana Oncology's clinical trial programs.
Illustrative Breadth of Responsibilities:
<ul>
<li>Radiolabeling/ coordination chemistry process, analytical development and troubleshooting with a broad range of radioisotopes, including but not limited to: Lu-177, Ac-225, Zr-89, Cu-64, In-111, Ga-68 and Pb-212.</li>
<li>Early formulation development, process and analytical method optimization to ensure drug product stability.</li>
<li>Participate in the development and process validation of radiopharmaceutical productionprocedures for use in preclinical and clinical studies.</li>
<li>Support CMC drafting and executing Master Batch Records, protocols for validation of manufacturing processes of radiopharmaceuticals, validation of analytical methods.</li>
<li>Participate and support CMC analytical development, method validation, and reporting activities, including but not limited to Identity, Purity, Impurities and Assays.</li>
<li>Support CMC in preparation of method validation protocols, execution of method validations, and authoring/review of reports, SOPs, and other technical documents for technical correctness, quality, and regulatory compliance.</li>
<li>Perform analysis, tabulating and gathering data for CMC sections (Module 3), development reports for IND and IMPD, to regulatory agencies including FDA and EMEA.</li>
<li>Support team communications in disseminating results, which may come in the form of presentations or reports.</li>
<li>Contribute to the organization and maintenance of the laboratory.</li>
</ul>
Requirements/Skills:
<ul>
<li>A Ph.D. in Inorganic Chemistry, Organic Chemistry, Radiochemistry, or related discipline and 0+ years of Biotech or Pharmaceutical industry experience; BS or MS in Chemistry or related discipline and 4 6+ years of Biotech or Pharmaceutical industry experience.</li>
<li>Radiopharmaceutical drug substance and drug product development experience is a plus.</li>
<li>Development experience for the biologics and peptides GMP manufacturing is a plus.</li>
<li>A strong background and in-depth working knowledge of biologics and peptides andconjugates analysis, including but not limited to: Assay and Purity (RP-HPLC, IP-RP-HPLC,AEX/CEX-HPLC), with LC-MS and LC-ICP-MS experience being a plus.</li>
<li>Knowledgeable in regulatory requirements and guidelines (cGMP, ICH, FDA, and USP, EP) with the ability to apply to the Phase appropriate pharmaceutical development. GMP pharmaceuticals validation experience is a plus.</li>
<li>Experience with regulatory documentation is preferred. </li>
<li>Understanding of chemistry manufacturing and controls (CMC) documentation for novelcompounds consistent with requirements for IND, NDA, or other regulatory pathways.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Strict adherence to data integrity is required. </li>
<li>Proven ability to adhere to good documentation standards and maintain detailed records of all work performed.</li>
<li>Excellent verbal and written communication skills.</li>
</ul>
Mariana Oncologys Values
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>
 
Mariana Oncology Compensation Summary:
The salary for this position is expected to range between $120,086.00 and $162,470.00 per year. Your compensation will also include a performance-based cash incentive.
The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and will be reviewed periodically upon joining Mariana Oncology. Mariana may change the published salary range based on company and market factors.
US-based eligible employees will receive a comprehensive benefits package that includes a strong health insurance package, life insurance, disability benefits, a 401(k) with company contribution and match, tuition reimbursement, and a variety of other benefits. In addition, employees are eligible for a generous flexible time off program.

Scientist I/II, CMC Radiochemistry

<h3>Job Description</h3>
Job DescriptionVoleon is a technology company that applies state-of-the-art AI and machine learning techniques to real-world problems in finance. For nearly two decades, we have led our industry and worked at the frontier of applying AI/ML to investment management. We have become a multibillion-dollar asset manager, and we have ambitious goals for the future.&nbsp;&nbsp;Your colleagues will include internationally recognized experts in artificial intelligence and machine learning research as well as highly experienced finance and technology professionals. &nbsp;The people who shape our company come from other backgrounds, including concert music performances, humanitarian aid, opera singing, sports writing, and BMX racing. You will be part of a team that loves to succeed together. In addition to our enriching and collegial working environment, we offer highly competitive compensation and benefits packages, technology talks by our experts, a beautiful modern office, daily catered lunches, and more. As a member of our Investor Relations and Business Development (IRBD) team within our Client Research and Marketing functions, you will create and maintain investor-facing content that explains our quantitative strategies to sophisticated institutional audiences. You will work closely with IRBD colleagues in Client Research, Marketing, and Sales, and collaborate with Research, Reporting, and Compliance, to help deliver insights that foster a deeper understanding of Voleon’s research and portfolios. You will turn data and research into clear narratives and visuals, strengthening our partnerships among the world’s leading institutional investors and contributing to capital growth efforts. This position is open to remote work in the US with the option to work hybrid or onsite at our offices in Berkeley or New York.Responsibilities
<ul>
<li>Work independently and collaboratively with senior team members to develop materials for investors, including presentations, fact sheets, investor letters, and thought-leadership pieces, with a strong emphasis on data-analysis, accuracy, clarity, and visual excellence</li>
<li>Help translate quantitative research and portfolio results into clear, accurate narratives and visuals for institutional investors</li>
<li>Own standard material updates, coordinating inputs across teams and ensuring timely, error-free delivery</li>
<li>Drive content from draft to final approval, incorporating feedback from leadership and teammates</li>
<li>Partner&nbsp;with&nbsp;sales, investment, and back/middle&nbsp;office teams to gather data and respond to RFIs, DDQs, and ad-hoc requests</li>
<li>Help design and enforce content style guidelines and templates to ensure consistency across communications</li>
<li>Work closely with Compliance to obtain necessary approvals and maintain required disclosures</li>
</ul>
Requirements
<ul>
<li>3+ years of experience working within the investment management industry</li>
<li>Outstanding organizational skills to set priorities, manage multiple deliverables in parallel and meet time sensitive deadlines</li>
<li>Excellent analytical rigor and&nbsp;robust&nbsp;attention to detail</li>
<li>Strong proficiency with PowerPoint and Excel, including experience using MS Office software to produce high quality presentations</li>
<li>Excellent oral and written communication skills</li>
<li>Bachelor’s degree</li>
</ul>
 Preferred Qualifications
<ul>
<li>Familiarity with&nbsp;hedge fund investment strategies and&nbsp;investing concepts</li>
<li>Exposure to financial databases or data delivery, e.g., Bloomberg</li>
<li>Ability to code in Python, R, or similar languages</li>
<li>CFA or CAIA or willingness to pursue these certifications</li>
</ul>
The base salary range for this position is&nbsp;$125,000 to $150,000&nbsp;in the location(s) of this posting. Individual salaries are determined through a variety of factors, including, but not limited to, education, experience, knowledge, skills, and geography. Base salary does not include other forms of total compensation such as bonus compensation and other benefits. Our benefits package includes medical, dental and vision coverage, life and AD&amp;D insurance, 20 days of paid time off, 9 sick days, and a 401(k) plan with a company match. “Friends of Voleon” Candidate Referral ProgramIf you have a great candidate in mind for this role and would like to have the potential to earn&nbsp;$7,500&nbsp;if your referred candidate is successfully hired and employed by The Voleon Group, please use this&nbsp;form&nbsp;to submit your referral. For more details regarding eligibility, terms and conditions please make sure to review the&nbsp;Voleon Referral Bonus Program.&nbsp;Equal Opportunity EmployerThe Voleon Group is an Equal Opportunity employer. Applicants are considered without regard to race, color, religion, creed, national origin, age, sex, gender, marital status, sexual orientation and identity, genetic information, veteran status, citizenship, or any other factors prohibited by local, state, or federal law. #LI-TN1&nbsp;
We may use artificial intelligence (AI) tools to support parts of the hiring process. These tools assist our recruitment team but do not replace human judgement. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Senior Associate, Client Research

<h3>Job Description</h3>
Job Description
Come join CCRM Fertility, a global pioneer in fertility treatment, research, science, specializing in IVF, fertility testing, egg freezing, preimplantation genetic testing, third party reproduction and egg donation. As a member of CCRM Fertility’s diverse team of professionals, you will be a part of helping families grow and changing lives. We take pride in providing our employees with meaningful employment, a supportive culture, and a well-balanced personal &amp; work life alignment. For more information, visit <a href="http://www.ccrmivf.com" target="_blank">www.ccrmivf.com</a>
Location Address: 
Department: IVFLaboratory
Work Schedule: Monday – Friday (8:00am – 4:30pm)
What We Offer Our Team Members:
<ul>
<li>Generous Paid time-off (PTO) and paid holidays</li>
<li>Medical, Dental, and Vision Insurance</li>
<li>Health benefits eligible the first day of the month following your start date.</li>
<li>401(k) Plan with Company Match (first of the month following 2 months of service)</li>
<li>Basic &amp; Supplement Life Insurance</li>
<li>Employee Assistance Program (EAP)</li>
<li>Short-Term Disability</li>
<li>Flexible spending including Dependent Care and Commuter benefits.</li>
<li>Health Savings Account</li>
<li>CCRM Paid Family Medical Leave (eligible after 1 year)</li>
<li>Supplemental Options (Critical Illness, Hospital Indemnity, Accident)</li>
<li>Professional Development, Job Training, and Cross Training Opportunities </li>
<li>Bonus Potential</li>
</ul>
What You Will Do:The Senior Embryologist will be responsible for performing all procedures in the IVF Laboratory under the direction of the IVF Laboratory Supervisor. The Senior Embryologist must demonstrate knowledge and skills related to the various procedures performed in the IVF Laboratory. The Senior Embryologist reports directly to the IVF Lab Supervisor.
<ul>
<li>Perform daily, weekly, and periodic function checks and maintenance on equipment and trouble shoot equipment problems and make appropriate decisions for repair, with guidance.</li>
<li>Follow appropriate blood borne pathogen handling and disposal procedures.</li>
<li>Perform all aspects of media/medium preparation with sterile technique for each case and documents the lots used.</li>
<li>Process semen for IVF procedures according to IVF lab protocol.</li>
<li>Assist physician during egg retrievals and is able to locate and assess all oocytes retrieved in a timely manner. Able to trim oocytes without trauma or injury to the oocytes.</li>
<li>Adhere to the IVF lab’s double signature and check system when performing procedures to ensure correct identity of eggs, sperm, and embryos.</li>
<li>Document all patients’ results into the IVF Lab information system (LIS).</li>
<li>Perform daily fertilization checks which includes “cleaning” embryos with minimal trauma (insemination cases) to observe fertilization.</li>
<li>Assess fertilization by observation of pronuclei and polar bodies.</li>
<li>Perform freezing and thawing of human embryos according to IVF lab protocol with a high survival rate.</li>
<li>Perform oocyte inseminations according to IVF lab protocol.</li>
<li>Able to hyal and strip oocytes for ICSI with minimal trauma.</li>
<li>Perform Intracytoplasmic Sperm Injection (ICSI) according to IVF lab procedures resulting in high fertilization rates.</li>
<li>Assist physician with embryo transfer and ensures proper identification of the patient with a “time-out” before the transfer.</li>
<li>Assist physician during PESA, MESA and TESE procedures by locating and processing sperm found according to IVF lab procedures.</li>
</ul>
<ul>
<li>Perform biopsy procedures, including trophectoderm biopsy, resulting in high number of embryos returning a test result. Embryos biopsied result in a high survival rate when thawed and an acceptable implantation rate when transferred.</li>
<li>Other duties as assigned.</li>
</ul>
What You Bring:
<ul>
<li>Bachelor’s Degree in Biology, Chemistry, or Microbiology required.</li>
<li>Medical technology licensure/certificate required if Embryologist completed a medical technology university-based program.</li>
<li>5+ years’ experience in laboratory or scientific research required (Med laboratory preferred).</li>
<li>Computer and database experience preferred.</li>
</ul>
Working Conditions:The physical demands described here are representative of those which should be met, with or without reasonable accommodation (IAW ADA Guidelines), by an employee to successfully perform the essential functions of this job. This job operates in a professional office and clinical setting. This role routinely uses standard office equipment such as computers, including computer keyboards and mice; telephones; photocopiers; scanners; filing cabinets. While performing the duties of this job, the employee is regularly required to communicate with others. The employee is frequently required to sit; will occasionally stand and/or walk; use hands and fingers to grasp, pick, pinch, type; and reach with hands and arms. Employees should have the visual acuity to perform an activity such as: preparing and analyzing data and figures, viewing a computer terminal, extensive reading, and operation of standard office machines and equipment. 
CCRM’s Compensation: The salary range represents the national average compensation for this position. The base salary offered will vary based on location, experience, skills, and knowledge. The pay range does not reflect the total compensation package. Our rewards may include an annual bonus, flexible work arrangements, and many other region-specific benefits.
Pre-Employment Requirements:All offers of employment are conditional upon the successful completion of the CCRM Fertility onboarding process, including verification of eligibility and authorization to work in the United States. This employer participates in the E-Verify Program in order to verify the identity and work authorization of all newly hired employees.
Equal Employment/Anti-Discrimination: We are an equal-opportunity employer. In all aspects of employment, including the decision to hire, promote, discipline, or discharge, the choice will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Senior Embryologist

<h3>Job Description</h3>
Job Description
EnSafe is seeking a Senior Hydrogeologist to join our team of environmental professionals working on complex and rewarding projects across the countrybased out of any of EnSafe’ soffices listed: Jacksonville, Tampa, Pensacola, FL; Houston, TX; Memphis, Knoxville, Nashville, TN; or Hartford, CT
EnSafe is an employee-owned global environmental consulting and engineering firm. We strive to provide cutting-edge, creative solutions for our clients. EnSafe specializes in custom solutions in Environmental Management and Planning, Civil Design Engineering, Environmental Restoration, Natural &amp; Water Resources, Health &amp; Safety, and Technology, with offices operating within the U.S. 
What We Are Looking For
As Senior Hydrogeologist, you will lead and contribute to multidisciplinary projects involving environmental site investigation, remediation, groundwater modeling, and regulatory compliance. We offer a workplace culture that promotes autonomy, continuous learning, and professional growth. 
What You Will Be Doing: 
<ul>
<li>Designing, directing, and executing complex site investigations, including the planning and implementation of drilling, geophysical logging, aquifer testing, sampling of various media, and installation of monitoring and recovery wells.</li>
<li>Leading project teams in developing conceptual site models and conducting contaminant fate and transport evaluations.</li>
<li>Managing and overseeing field activities, ensuring health and safety compliance, subcontractor coordination, and efficient scheduling.</li>
<li>Interpreting hydrogeologic data and synthesizing field and analytical results to support reporting, risk assessments, remedial design, and regulatory decision-making.</li>
<li>Practical use of advanced groundwater models to support site characterization and remediation/optimization strategies.</li>
<li>Writing and reviewing technical reports, work plans, sampling plans, and standard operating procedures (SOPs).</li>
<li>Serving as a technical advisor, mentoring junior staff, performing quality control reviews, and helping the next generation of hydrogeologists grow.</li>
<li>Interfacing with clients and regulatory agencies as a subject matter expert, providing strategic guidance, presenting findings, and supporting negotiations.</li>
<li>Performing optimization of passive and active remedial alternatives, including LTM.</li>
<li>Building, calibrating, and validating analytical and numerical soil, groundwater, surface water, sediment, and indoor air (attenuation) modeling.</li>
<li>Providing litigation support for discovery, affidavits, deposition, and trial.</li>
<li>Performing sequence stratigraphy evaluations and reporting.</li>
<li>Performing statistical evaluations, background studies, and associated reporting.</li>
<li>Travel up to approximately 30% may be required, including occasional overnight trips.</li>
</ul>
What You Will Need:
<ul>
<li>Bachelor's or Master’s degree in Hydrology, Hydrogeology, Geology, Engineering, or a closely related field.</li>
<li>15–20 years of professional experience, preferably in environmental consulting. </li>
<li>Professional Geologist or Engineer licensure (by exam).</li>
<li>Strong background in hydrogeologic site characterization, groundwater flow and transport modeling and analysis, and environmental remediation/remedy optimization.</li>
<li>Proficiency with regulatory programs including CERCLA, RCRA, and state-specific programs.</li>
<li>Demonstrated ability to lead projects and teams, manage multiple priorities, mentor/supervise employees, and communicate effectively with diverse audiences.</li>
<li>Advanced skills in data analysis, report writing, and preparation of maps, tables, charts, and figures.</li>
<li>Experience using hydrogeologic modeling tools, including but not limited to MODFLOW, MT3D codes, VISTAS, EVS, etc. </li>
<li>Familiarity with GIS applications.</li>
<li>Excellent verbal and written communication skills. </li>
<li>Current 40-hour HAZWOPER certification.</li>
</ul>
About EnSafe
EnSafe began as a two-person firm in 1980, navigating complex regulatory compliance issues on behalf of our clients. We nurture our people with growth and development opportunities. We build enduring, trustful relationships with each of our clients, with a focus on high ethical and safety standards. We build this reputation by attracting high-quality people and retaining them for the long term.
At EnSafe, we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right candidate for this or other roles at our company.
EnSafe is committed to being an EEO employer and all qualified candidates will receive consideration without regard to race, color, religion, national origin, citizenship, age (except for bona fide occupational qualifications), sex, disability, sexual orientation, gender identity, marital status, military or veteran status, any other status protected by federal, state, or local law, or association with a person on the basis of one or more of the foregoing.
Check us out on the web at <a href="http://www.ensafe.com" target="_blank">www.ensafe.com</a>

Senior Hydrogeologist

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite at a NEFSC Facility
POSITION DESCRIPTION:
Think Tank is a woman-owned small business with more than 27 years of proven success delivering exceptional IT and marine fisheries services to the federal government. We are currently seeking an ideal candidate for the position of Statistician to support an upcoming proposal with the National Oceanic and Atmospheric Administration. Résumé of successful candidate(s) will be included with our proposal. 
The Statistician supports the development and application of statistical models to evaluate the abundance, distribution, and population dynamics of marine mammals, sea turtles, and other protected species. This role is essential in supporting assessments that guide federal conservation and management decisions.
RESPONSIBILITIES:
<ul>
<li>Apply statistical methodologies (e.g., generalized linear models, distance sampling, Bayesian approaches) to ecological and survey data.</li>
<li>Contribute to the development of models for abundance estimation, bycatch estimation, and ecological trend analysis.</li>
<li>Collaborate with biologists and analysts to support survey design, population assessments, and environmental data integration.</li>
<li>Assist in preparing technical reports, peer-reviewed manuscripts, and permit documentation.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Bachelor's or Master's degree in statistics, quantitative ecology, or a related field.</li>
<li>Proficiency in R, Python, and/or SAS, with experience in modeling ecological data.</li>
<li>Familiarity with survey data, spatial analysis, and statistical inference methods.</li>
<li>Excellent problem-solving, documentation, and communication skills.</li>
<li>Experience contributing to scientific publications or technical reports </li>
</ul>

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