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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.

• 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.

The Medical Director oversees clinical trials, data collection, and protocol implementation. Manages program development, working cross-functionally with various disciplines. Supports data analysis and contributes to the preparation of abstracts, presentations, and manuscripts.

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

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.

• 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.

Accountable for the operational management and execution of global clinical trial programs (Phases I-III). Ensure adherence to GCPs, SOPs and all regulatory agency guidelines, as well as study operational planning and execution. Partner with CROs and other 3rd party vendors to oversee and ensure study milestones and deliverables are achieved according to agreed quality standards and timelines.

Apogee Therapeutics is a biotechnology company seeking to develop differentiated biologics for the treatment of inflammatory and immunology indications.

• Lead Braveheart’s global PV strategy and partner closely with Clinical, Regulatory, and other development functions.
• Lead all PV contributions to Investigational New Drug (IND) and Clinical Trial Application (CTA) submissions worldwide, with responsibility for developing high-quality safety sections.
• Shape the future PV function— its people, structure, and operating model— as Braveheart transitions from clinical development to post-market commercialization.

Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease.

• 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.

• 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.

• 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.

• Assist with the development of the protocol and informed consent form and/or program design.
• Manage vendor budgets, payments, and timelines.
• Effectively track and report on internal project metrics and study progress.

Tonix is a fully integrated biotechnology company, publicly traded on NASDAQ (ticker: TNXP), with marketed products and a pipeline of development candidates. They are focused on commercializing, developing, discovering, and licensing therapeutics to treat and prevent human disease and operates a state-of-the art infectious disease research facility. They provide a comprehensive compensation and benefits package.

• Lead a team of biostatisticians in the design, analysis, and interpretation of clinical studies within oncology.
• Drive strategic biostatistical decisions and collaborate with stakeholders to deliver clinical insights.
• Develop and implement novel statistical methods to support innovative study designs, ensuring high-quality statistical deliverables.

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

• 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.

• Lead complex clinical trials from initiation through completion.
• Oversee cross-functional teams and manage project scope.
• Contribute to high-impact clinical research projects.

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

• 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.

• Lead and manage complex clinical oncology projects.
• Coordinate cross-functional activities and external vendors.
• Guide project planning, risk management, and compliance efforts.

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

• Lead and mentor a team of biostatisticians in oncology clinical validation projects.
• Develop and implement novel statistical methods for innovative study designs.
• Ensure scientific rigor and high-quality documentation for internal and external stakeholders.

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements.

• Support operational planning, start-up, execution, and close-out activities for Phase 3 clinical studies in HCM.
• Oversee CROs, vendors, clinical sites, and external partners to ensure delivery of high-quality data, adherence to timelines, and compliance with GCP and regulatory requirements.
• Lead selection, onboarding, and oversight of CROs, central labs, imaging vendors, and specialty service providers.

Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease.

• Serve as a primary scientific and operational point of contact for Praxis clinical trial sites.
• Deliver protocol and investigative product training to site personnel.
• Identify and help resolve site-level issues related to patient recruitment and retention.

Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders.

As Clinical Trial Manager, you will lead CRAs and oversee clinical aspects of studies across multiple countries. You will ensure timeline adherence and scope, whilst ensuring quality delivery. Management and operational delivery of the clinical elements within a trial including site selection, start-up, and data cleaning activities. Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor.

Precision for Medicine is a precision medicine CRO which combines novel clinical trial designs, experts and biomarker solutions.