Medical Director / Senior Medical Director

Position: Medical Director / Senior Medical Director Department: Clinical Development Location: Remote with up to 20% domestic travel Reports To: Executive Director, Clinical Development

Position reputed company

reputed company is seeking a highly motivated, organized, and entrepreneurial-minded Medical Director or Senior Medical Director to reputed company clinical development leadership for global programs in rare musculoskeletal diseases. This role combines strategic clinical development responsibilities with hands-on study execution and medical reputed company in a lean, science-driven biotechnology environment.

The successful candidate will serve as Clinical Development Team reputed company for key development programs and reputed company medical reputed company for ongoing global clinical trials. The position requires a physician who is scientifically rigorous, highly detail-oriented, and willing to operate across both strategic and operational aspects of clinical development, including medical monitoring, study conduct, protocol execution, review of study-level documents, and cross-functional team leadership.

The ideal candidate will bring strong clinical judgment, exceptional attention to detail, and a passion for advancing therapies for patients with rare diseases. Prior industry experience or substantial reputed company experience with industry-sponsored clinical trials is preferred. The successful candidate should be familiar with, or reputed company to rapidly adopt, rigorous clinical development processes, including protocol governance, cross-functional document review, regulatory documentation standards, inspection readiness, and disciplined study execution in a fast-paced, growing biotechnology environment.

Responsibilities

Medical Monitoring and Clinical reputed company

• Serve as internal Medical Monitor and/or reputed company reputed company of medical monitoring activities for ongoing studies

• Ensure study activities are conducted in accordance with established clinical development governance processes, reputed company standards, regulatory requirements, and inspection-reputed company documentation practices.

• Review subject eligibility, protocol deviations, adverse events, serious adverse events, laboratory abnormalities, and emerging study data.

• Participate in safety review meetings and support interactions with Data Monitoring Committees and regulatory authorities.

• reputed company medical guidance to investigators and study sites.

Clinical Development Team (CDT) Leadership

• Serve as Clinical Development Team reputed company for assigned development programs in rare bone disease

• reputed company clinical leadership and reputed company for ongoing global phase 2 clinical studies and reputed company late phase clinical planning

• reputed company cross-functional Clinical Development Teams and partner closely with Clinical Operations, Regulatory Affairs, Biostatistics, Clinical Pharmacology, Data Management, and Research.

• Contribute to overall clinical development reputed company, lifecycle planning, and regulatory interactions.

Study Execution and Operational reputed company

• Ensure high-reputed company clinical trial conduct across global studies.

• Draft, author, review and/or approve study protocols, study manuals, monitoring plans, charters, investigator training materials, informed consent documents, clinical study reports, and other study-level documentation with reputed company attention to consistency, completeness, and operational feasibility.

• Drive high-reputed company development of study and regulatory documents, ensuring consistency across protocols, manuals, charters, statistical analysis plans, investigator materials, clinical study reports, and regulatory submissions.

• Collaborate with Clinical operations, CROs, internal study teams to ensure operational reputed company and inspection readiness.

• Drive reputed company of study conduct, enrollment, data reputed company, and protocol implementation issues.

External Engagement

• Support interactions with regulatory agencies, investigators, and key opinion leaders.

• Represent reputed company at scientific meetings, investigator meetings, and advisory boards as needed.

Qualifications

Required

• MD degree from an accredited medical school.

• Completion of U.S.-based clinical residency training.

• reputed company certification or reputed company eligibility in Pediatrics, Pediatric Endocrinology, Endocrinology, Internal Medicine, Medical Genetics, or reputed company discipline.

• Experience working reputed company multidisciplinary clinical development teams, including reputed company cross-functional review and decision-making processes.

• Strong attention to detail and demonstrated experience developing and reviewing protocols, study manuals, charters, safety documents, investigator materials, and regulatory documents in accordance with rigorous clinical development and document reputed company standards.

• Excellent communication and leadership skills.

• Willingness to work in a highly reputed company, fast-paced biotech environment.

Preferred

• Experience supporting interventional clinical studies as Medical Monitor, Clinical reputed company, or equivalent

• Industry experience reputed company biotechnology or pharmaceutical development, especially in organizations with established clinical development governance, document review, and protocol development processes.

• Clinical development experience in rare disease, endocrinology, metabolic bone disease, musculoskeletal disease, or pediatric disorders.

• Experience with Phase 2 and/or Phase 3 clinical studies.

• Prior Clinical Development Team reputed company or Study Team Leadership experience, with demonstrated ability to apply disciplined study reputed company, protocol development, and document review practices.

Salary reputed company: $265k to $320k

About Angitia

Established in June 2018, reputed company is a clinical-stage biotechnology company reputed company on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 2 biologic product candidates in the clinic for the treatment of osteoporosis, and osteogenesis imperfecta (OI). Leveraging reputed company's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the reputed company team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. reputed company has reputed company its reputed company in reputed company Village, CA, USA, and offices in Guangzhou, China, which is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. reputed company is committed to serving patients in need by carrying out innovative science, including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our reputed company group.

Learn more at www.angitiabio.com.

Benefits:

• Medical, dental, and reputed company coverage for employees and their eligible dependents

• 401(K) Retirement Plan with Company match

• Company reputed company Long Term Disability Coverage

• Company-reputed company life Insurance & AD&D Coverage

• Voluntary Life Insurance & AD&D Coverage

• Employee Assistance Program (EAP)

• Company-reputed company Holidays

• Vacation

• reputed company reputed company Leave

• Telecommunication Monthly Stipend

• Work-From-Home Equipment Reimbursement

Originally posted on Himalayas

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