Lead clinical trial strategies and evidence-generation plans supporting global regulatory submissions.
Design and oversee clinical protocols, claims, and evidence strategies in collaboration with internal and external stakeholders.
Serve as a scientific liaison with regulatory authorities and mentor junior scientists to drive clinical excellence.
The company develops diagnostic products for the US and EU markets, focusing on generating robust clinical evidence for regulatory submissions. It maintains a remote-first culture with a collaborative, cross-functional environment and opportunities for scientific leadership.
Lead the Scientific Program Management function, establishing practices, standards, and operating rhythms for program execution.
Partner with scientific and organizational leadership to align program priorities, manage risks, and provide portfolio visibility.
Directly manage and develop a team of Scientific Program Managers, fostering a culture of collaboration and continuous improvement.
Sage Bionetworks is a nonprofit that uses open science and collaboration to improve human health. They are a mission-driven, distributed team of scientists, engineers, and governance experts.
Own the full sales cycle for research-grade products and manufacturing solutions, from lead generation to deal closure.
Collaborate with technical sales teams to support technical qualification and value-based selling for cell and gene therapy.
Build and grow customer relationships while maintaining a disciplined sales funnel and meeting revenue targets.
The hiring company is a life sciences partner of Jobgether, providing research-grade products and manufacturing solutions. The culture emphasizes remote work and collaboration across technical and sales teams to support drug development.
Monitor clinical trial sites to ensure compliance with protocols, SOPs, and regulatory requirements.
Review electronic medical records and source documentation for accuracy and data integrity.
Support site staff and contribute to development of trial materials, SOPs, and training guides.
Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies to improve transplant outcomes for blood cancer patients. The company maintains a start-up culture with an entrepreneurial spirit and emphasis on camaraderie.
Establish and maintain relationships with investigators, sites, and key opinion leaders to support trial execution.
Gather site feedback and translate it into actionable improvements for study teams.
Contribute to protocol development, site selection, and business development activities.
This role is with a partner company that focuses on clinical research and trial execution. The company operates remotely and values collaboration, inclusion, and professional autonomy.
Support operational execution of clinical studies from initial synopsis through final deliverables.
Manage implementation, on-time execution, and conduct of clinical studies, including budget and vendor management.
Oversee cross-functional study teams and ensure compliance with regulations and data integrity.
Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. They are committed to continuous innovation in cell therapy.
Manage business operations for multiple scientific teams in the Pacific Northwest, including Washington and Colorado.
Lead direct reports, group leaders, and teams, and serve clients in technical settings like laboratories.
Collaborate with clients to meet resourcing needs, ensure high-quality service, and handle financial responsibilities as defined by the Director.
Eurofins Scientific is an international life sciences company providing analytical testing services to ensure safety and sustainability across industries. With 58,000 staff and 900 laboratories in over 54 countries, it operates as a decentralized and entrepreneurial network, offering over 200,000 testing methods.
Support Clinical Trial Managers with study start-up, protocol development, and Trial Master File preparation.
Coordinate with clinical sites on documentation, training, and compliance with FDA and GCP requirements.
Assist with tracking study payments and providing operational support across the full study lifecycle.
The company is a partner organization specializing in clinical research and development, operating through Jobgether. It offers a structured clinical operations environment with cross-functional teams and professional growth opportunities.
Lead and coordinate end-to-end FRO launches, bringing together legal, finance, people, IT, and more.
Run founder programs, including residencies and open calls, from planning to closeout.
Serve as a trusted partner to founders, advocate for their needs, and help build launch systems.
Convergent Research is a nonprofit science studio that designs, launches, and supports mission-driven organizations focused on scientific and engineering bottlenecks. The company has taken 14 FROs from idea to operating entity, including four launches in 2026, and values an inclusive, respectful workplace.
Drive sales performance across laboratory product categories including lab weighing, liquid handling, filtration, and microbiology.
Manage a remote territory covering Texas, Oklahoma, and New Mexico, with autonomy and strategic account planning.
Collaborate with cross-functional teams to expand market presence and accelerate growth in the life sciences sector.
The company is a global life sciences organization providing laboratory products, services, and solutions. They emphasize collaboration, sustainability, and a people-first culture, supporting scientific research and improved health outcomes.
Perform lead biostatistician role providing technical expertise for complex clinical studies.
Develop statistical sections of protocols, analysis plans, and review tables/figures for regulatory submissions.
Partner with statistical programmers to manage timelines and ensure quality deliverables.
Freenome is developing in vitro diagnostic products for early cancer detection through blood tests. The company values diversity and fosters a collaborative, fast-paced culture.
Lead disease awareness and relationship development with key experts for EBV+ PTLD in preapproval phase.
Drive demand and support treatment experience of Tab-cel post-approval within assigned territory.
Navigate complex accounts, collaborate cross-functionally, and create strategic account plans.
Pierre Fabre is a private French multinational pharmaceutical and dermo-cosmetics company. It is one of the world's largest dermo-cosmetics companies and a leading European pharmaceutical laboratory, recognized by Forbes as a top employer.
Support NIAID's Small Business Program and SBIR/STTR activities, assisting applicants and communicating with biomedical small businesses.
Analyze extramural small-business biomedical research in infectious diseases, immunology, and HIV/AIDS.
Coordinate outreach programs and develop web content, FAQs, and success stories to attract and retain small biomedical businesses.
Integres, LLC is a Service-Disabled Veteran Owned Small Business that provides high-quality, agile information technology-based solutions. They cultivate a corporate family culture emphasizing excellence, accountability, and work/life balance.
Lead biostatistics activities across clinical studies, ensuring high-quality analyses and clear communication.
Provide statistical expertise for oncology trials, from protocol development to regulatory submissions.
Oversee statistical programming and deliverables, ensuring quality, integrity, and compliance.
Jobgether is a platform that uses AI-powered matching to connect candidates with hiring companies, focusing on objective and fair application reviews. The company is dynamic and emphasizes a streamlined hiring process, with a data-driven approach and a commitment to innovation.
Manage end-to-end IRB meeting workflows, including submissions, reviewer assignments, and meeting preparation.
Facilitate communication among client services, IRB Chairs, Board members, and clients to ensure timely review processes.
Prepare and review informed consent forms for regulatory compliance and quality.
The company coordinates Institutional Review Board (IRB) meetings within a highly regulated clinical research environment. They offer a collaborative and inclusive culture focused on ethical, patient-centered outcomes, though company size is not specified.
Identify real cancer-biology datasets and convert them into rigorous, deterministically-graded tasks for AI agents.
Establish defensible reference analyses and scoring criteria across conclusion types from basic biology to clinical outcomes.
Anticipate plausible agent errors and test handling of experimental variability, incomplete data, and conflicting evidence.
Latch builds rigorous scientific benchmarks for AI agents in biology, partnering with frontier labs and pharma. The team emphasizes cross-domain integration, long-horizon reasoning, and a culture of respectful debate and flexible schedules.
Provide statistical expertise across clinical development programs, authoring SAPs and overseeing ADaM/TFL deliverables.
Contribute to innovative trial designs, regulatory submissions, and cross-functional collaboration with clinical teams.
Ensure high-quality statistical analyses and compliance with regulatory requirements in a remote/hybrid setting.
The partner company specializes in global clinical development, supporting registration-directed clinical trials across therapeutic areas. It fosters a collaborative, results-oriented culture with a focus on innovation, professional growth, and high-quality deliverables.
Provides operational leadership for global clinical trials, overseeing the clinical operations team and vendor performance.
Ensures effective study delivery through cross-functional collaboration, proactive risk management, and strong execution oversight.
Manages CROs, vendors, and strategic partners, driving financial accountability and maintaining inspection readiness.
Summit Therapeutics Inc. is a biopharmaceutical oncology company focused on improving quality of life and resolving serious unmet medical needs. With multiple global Phase 3 clinical studies, the company is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Support quality assurance for PGT laboratory and genetic counseling protocols, applying clinical and molecular genetics expertise.
Manage complex domestic and international PGT-M and PGT-SR cases from enrollment through test completion.
Contribute to product improvements, quality initiatives, data analysis, and operational projects.
They provide high-quality genomic and reproductive genetic testing services. The company is a collaborative, science-driven organization with a focus on quality and innovation.
Engage with patients to recruit, educate, and pre-screen them for clinical studies.
Maintain data accuracy across multiple study portals and manage data entry and queries.
Collaborate with site teams and PIs to ensure protocol compliance and resolve issues.
Care Access brings world-class research and health services directly to communities, working to make the future of health better for all. With hundreds of research locations and a global team, we are dedicated to ensuring every person can contribute to medical breakthroughs.