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Serve as the project physician and provide medical oversight for oncology clinical trials. Collaborate with cross-functional teams to guide project execution. Monitor patient safety and clinical data to ensure compliant trial outcomes.

Jobgether is a Talent Matching Platform that partners with companies worldwide to efficiently connect top talent with the right opportunities through AI-driven job matching.

• Serve as the project physician and provide medical and scientific expertise to project teams.
• Ensure the accuracy and integrity of trial data, with a focus on patient safety.
• Support business development activities, including proposal preparation and bid defense meetings.

Precision Medicine Group is an Equal Opportunity Employer.

• The Medical Director serves as the project physician and provides medical and scientific expertise to project teams, ensuring data accuracy and patient safety.
• Support Business Development by participating in the RFP process, preparing medical considerations for proposals, and participating in bid defense meetings.
• Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports and new drug applications.

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. They integrate clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step.

• Medical expert with specialized therapeutic expertise.
• Maintain consultative relationship with clients.
• Provide medical expertise / leadership in Proposal Development Teams.

Parexel improves world health. They provide biopharmaceutical services, helping clients transform scientific discoveries into new treatments, with values like Patients First, Quality, Respect, Empowerment & Accountability.

• Support development and communication of medical plans.
• Lead the development and dissemination of scientific and medical data.
• Build and maintain strong relationships with KOLs, researchers, and patient advocacy groups.

Jade Biosciences is focused on developing innovative therapies for autoimmune diseases. They are developing JADE101 to treat IgAN and have a second development candidate as well as an undisclosed antibody discovery program in preclinical development.

• Represent Iovance Medical Affairs as a TIL cell therapy expert in both internal and external venues.
• Provide high quality clinical input and review of disease strategy plans, slides, manuscripts and educational materials.
• Partner with Scientific Communications to develop timely publication strategies and plan, gap analysis, and key messages.

Iovance Biotherapeutics is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, their employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law.

The Medical Science Liaison will provide clinical and scientific information in response to inquiries about Iovance Biotherapeutics developmental products. They will identify, develop, and maintain relationships with regional and national key opinion leaders and support clinical trial site identification and execution. They will collaborate with other field-based personnel to ensure that Iovance maintains a strong clinical and scientific presence in the field.

Iovance Biotherapeutics is committed to cultivating and offering a diverse and inclusive work environment as an equal-opportunity employer.

• Develop, manage, and execute global clinical studies.
• Ensure timely and budget-compliant trial activities in accordance with quality standards.
• Lead the selection and oversight of clinical trial sites.

This position is posted by Jobgether on behalf of a partner company.

• Provide clinical scientific leadership for the clinical development organization.
• Lead the design and writing of clinical protocols and associated clinical documents.
• Represent Immunovant externally and build successful relationships with multiple stakeholders including trial site Investigators, KOLs, and others.

Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.

• Develop educational content consistent with overall brand strategy to drive impactful peer to peer engagements.
• Lead national and regional peer to peer programming and execution, including development of speaker program materials and coordination with sales leads.
• Partner with Medical Affairs to provide commercial perspective on publications, scientific communications, and real-world evidence/ HEOR data generation.

Iovance Biotherapeutics is a leading innovator in the cell therapy industry. They are passionate about saving lives and fostering a collaborative, inclusive environment.

• Manage complex medical issues and coordinate care, facilitating diagnostic and therapeutic treatment options worldwide.
• Offer high-level clinical management and education to clients and families in a compassionate manner.
• Collaborate with clinical and research teams to identify therapies and deliver information on medical conditions, treatments, and trials.

Private Health Management (PHM) supports people with serious and complex medical conditions, helping them obtain the best possible medical care. Trusted by healthcare providers and businesses, PHM offers independent, science-backed insights to help clients make informed decisions and access the best care.

The Director of Clinical Development leads the team responsible for design, execution, and strategic direction of clinical programs across Loyal’s veterinary product portfolio. This role drives end-to-end clinical strategy, from target product profile to study design and regulatory-facing protocol development through field execution, data interpretation, and evidence package generation. This is a highly cross-functional role that partners closely with Veterinary Affairs, Clinical Operations, Regulatory (FDA-CVM),CMC, and Commercial.

Loyal is a clinical-stage veterinary medicine company developing drugs intended to extend the lifespan and healthspan of dogs.

The Upstream Senior Clinical Program Manager will design and execute pre-market feasibility and pivotal clinical studies, ensuring regulatory compliance while supporting marketing claims. This role requires close collaboration with physician collaborators and internal stakeholders to collect, analyze, and interpret clinical data. The role offers remote flexibility, with occasional travel for on-site meetings and conferences.

This position is posted by Jobgether on behalf of a partner company.

• Drive scientific engagement and support clinical research.
• Partner with key opinion leaders and field sales Medical Science Liaisons.
• Ensure scientific accuracy and alignment with company strategy.

Karius is a life science, venture-backed clinical metagenomics company, focused on elevating patient care through microbial insights.

• Collaborate with cross-functional teams to develop clinical documents for dermatology-related trials.
• Contribute scientific input and implementation into study design and execution.
• Analyze clinical trial data, interpret results, and provide scientific insights to guide decision-making.

Apogee Therapeutics, Inc. is a biotechnology company seeking to develop differentiated biologics for the treatment of atopic dermatitis.

Manage clinical trials from inception to Clinical Study Report completion to drive meaningful change for patients and healthcare providers. Author and implement operational plans for efficient study enrollment and monitoring activities. Participate in audits and regulatory inspections as needed.

This position is posted by Jobgether on behalf of a partner company.

• Monitor and own the progress of clinical studies at investigative sites.
• Coordinate all necessary activities required to set up and monitor a study.
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.

Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences to improve the speed, cost and success rate of bringing life-changing therapies to patients. They have a strong focus on Oncology and Rare Disease and boast extremely high CRA retention rates compared to industry averages.