A biopharmaceutical company is seeking a Senior Medical Director for US Medical Affairs. This role involves executing Medical Affairs programs, supporting key relationships with external experts, and delivering medical expertise across multiple departments. Candidates must possess an M.D. degree and preferably have ...

Senior Medical Director-Oncology Global Medical Affairs, Multiple Myeloma Johnson & Johnson Oncology Global Medical Affairs is recruiting for a Senior Medical Director for Multiple Myeloma. The preferred locations are Bridgewater/Raritan, NJ, with remote work options considered on a case‑by‑case basis if approved b...

Your Future Evolves Here Evolent partners with health plans and providers to achieve better outcomes for people with most complex and costly health conditions. Working across specialties and primary care, we seek to connect the pieces of fragmented health care system and ensure people get the same level of care and ...

A biopharmaceutical company is seeking a Senior Medical Director for US Medical Affairs. This role involves executing Medical Affairs programs, supporting key relationships with external experts, and delivering medical expertise across multiple departments. Candidates must possess an M.D. degree and preferably have ...

A leading oncology diagnostic company is seeking a Medical Director to provide medical expertise across its oncology portfolio, focusing on melanoma and immunotherapy applications. This role requires an MD with board certification in Medical Oncology and at least 5 years of oncological experience. Responsibilities i...

skokie is a village in cook county, illinois, neighboring the city of chicago's northern border. skokie lies approximately 15 miles north of chicago's downtown loop. its name comes from a potawatomi word for 'marsh.' for many years, skokie promoted itself as 'the world's largest village.' as the premier staffing ag...

Pfizer is seeking a Clinical Development Medical Executive Director in Pennsylvania to drive the strategy for gastrointestinal cancer programs. This role involves leading clinical trials and collaborating with cross-functional teams while ensuring successful execution of development plans. The ideal candidate will ...

Caidya is seeking a Medical Director for Oncology to lead medical monitoring across global clinical trials. This role offers the chance to work with innovative cancer therapies and requires extensive oncology experience. The ideal candidate will have a strong clinical background, excellent decision-making abilities...

Medical Oncology Medical Director - Hoyt-Hunter Center for Oncology CareSouthwestern Vermont Medical Center (SVMC), a member hospital of Dartmouth Health (DH), and in collaboration with Dartmouth Cancer Center (DCC), is seeking an experienced, collaborative physician leader to serve as Medical Oncology Medical Direc...

The Oncology Field Medical, Director is responsible for providing therapeutic area/product expertise, including hematology and pipeline, across a broad range of medical customer segments and initiatives in an assigned territory (which could include Delaware, Maryland, Pennsylvania, North Carolina, South Carolina, Vi...

Hematology/ Oncology at the Alan B. Pearson Cancer Center is located in Lynchburg, Virginia and is seeking a board-eligible or board-certified physician to join a group of diverse and passionate providers. The group is the community's #1 most referred practice.The recently renovated 75,000+ square foot Alan B. Pears...

A healthcare recruitment firm is seeking a Director of Oncology Medical Affairs for a home-based role in the Western US. The ideal candidate is an MD with a background in oncology and a strong clinical skill set. Responsibilities include engaging with key opinion leaders, providing medical expertise, and managing tr...

About Us… Obsidian Therapeutics is pioneering engineered cell and gene therapies to deliver transformative outcomes for patients. Obsidian’s programs apply our cytoDRiVE® technology in Cell and Gene therapy products to control expression of proteins for enhanced therapeutic efficacy and safety. Obsidian’s lead prog...

Beam Therapeutics is looking for a Senior Manufacturing Associate in Durham, NC, focused on scaling cGMP manufacturing at its RTP site. The role requires at least 4-6 years of experience, especially in cell or gene therapy, and proficiency in tools like SAP and Veeva. Responsibilities include supporting GMP producti...

Job Responsibilities • Development of protocols for clinical studies. • Preparation of clinical development plans. • Drafting of clinical scientific documents such as IND, IND amendments, Investigator’s Brochures, Annual Reports and other FDA submissions. • Monitor, perform data review, and summarize safety and effi...

Job Description The Genitourinary and Melanoma Vice President is responsible and accountable for the overarching late-stage development plan for our company's assets in these disease areas. The Vice President (VP) will also be responsible and accountable for the end-to-end lifecycle management of selected assets. ...

Make it Happen at Hopkins! The cancer specialists at Sibley Memorial Hospital provide surgical, radiation and medical oncology and inpatient oncology services in Washington, D.C. metro area. As part of the Sidney Kimmel Comprehensive Cancer Center (hopkinsmedicine.org) patients are able to receive the world renown...

Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast cancer and beyond. It’s an exciting time to be part of Team Olema, with our transformation into a fully integrated oncology company well underway, top-lin...

Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard of care and improving outcomes for patients living with breast cancer and beyond. It’s an exciting time to be part of Team Olema, with our transformation into a fully integrated oncology company well underway, top-lin...

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who...

The Clinical Risk Liaison serves as the primary connection between the Transition and Clinical Teams and the Quality and Patient Safety Department. Reporting to the Director of Risk Management and Patient Safety, this role is charged with proactively identifying, prioritizing, and mitigating safety risks throughout ...

Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties. With internationally renowned centers of exc...

American Oncology Management Company seeks a Histology Technologist responsible for specimen processing and quality assurance in the laboratory. Key duties include processing and staining patient specimens, adhering to SOPs, and maintaining equipment. A Bachelor's Degree in a relevant field and a Florida Clinical L...

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who...

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who...

Location: Edgemont Senior Scientific Director, Clinical Safety (Oncology) At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immu...

Position Summary As a senior leader within Global Safety, the Senior Scientific Director, Clinical Safety (Oncology) provides strategic scientific leadership and oversight of clinical safety and pharmacovigilance activities across assigned oncology assets. This role is accountable for driving safety strategy, enabl...

Iovance Biotherapeutics, Inc. is seeking a Director, Regulatory CMC to lead drug development programs with a focus on global regulatory strategy and submissions. The successful candidate will collaborate with cross-functional teams and ensure compliance with evolving regulations. A minimum of 10 years in regulatory...

Position: Senior Regulatory Affairs – Oncology | Equity + Flexible PTO About us: Our purpose at Dispatch is to help create a world where all cancer patients can be cured. We’re humbled by the opportunity to work together as a team on some of the most pressing medical challenges of our time. To achieve our purpose...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is tr...

Director / Senior Director Global Regulatory Lead (Oncology) About the OpportunityOur client is a research-driven biopharmaceutical organization dedicated to advancing innovative therapies for patients with serious diseases worldwide. With a strong commitment to scientific excellence and patient impact, the company ...

US Oncology Inc. is seeking a qualified professional in Calverton, Maryland to oversee regulatory and administrative activities for clinical trials. This role requires a keen attention to detail and a deep understanding of regulatory compliance within oncology practices. The ideal candidate should possess at least ...

Cytel is seeking a Principal Statistician to lead statistical teams and provide expertise for clinical trials in Delaware. The candidate will support drug development, particularly in Oncology studies. With a strong requirement for a Master’s degree and at least 6 years in the pharmaceutical industry, this role dem...

Location: City of Albany Cytel is looking for a Principal Biostatistician to lead statistical support for clinical trials dedicated to major pharmaceutical clients. This role offers an opportunity to influence clinical development plans and oversee statistical outputs across trials. The ideal candidate will have a...

Join Sumitomo Pharma in Tallahassee as a key member of the oncology biostatistics team. You will lead statistical efforts for clinical projects, manage documentation, and mentor junior biostatisticians. The role requires a strong understanding of statistical methods, particularly in oncology trials, and excellent co...

Who Are You? As a Principal Statistician, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to lead and support clinical trials for drug development, with the opportunity to leverage your experience in late-phase trials and regulatory submissions for Oncology studies. ...

Principal Biostatistician Consultant- Remote in US (Oncology) United States Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice is searching for a Pri...

Sumitomo Pharma in Oklahoma City is looking for a Clinical Data Manager to oversee oncology clinical data management activities. This role is responsible for ensuring high-quality, compliant clinical trial data and collaborates cross-functionally to support clinical development programs. The ideal candidate will hav...

Acrivon Therapeutics, Inc. is seeking a Clinical Trial Manager to oversee the ARC-386 Phase II clinical trial in Watertown, MA. The successful candidate will manage site initiation, subject enrollment, and ensure compliance, while also managing study budgets and contracts. This role demands strong project managemen...

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