Clinical Development Team (CDT) Leadership

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

• Provide clinical leadership and oversight for ongoing global phase 2 clinical studies and future late phase clinical planning

• Lead 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 strategy, lifecycle planning, and regulatory interactions.

Study Execution and Operational Excellence

• Ensure high-quality 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 close attention to consistency, completeness, and operational feasibility.

• Drive high-quality 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 excellence and inspection readiness.

• Drive resolution of study conduct, enrollment, data quality, and protocol implementation issues.

External Engagement

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

• Represent the 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.

• Board certification or board eligibility in Pediatrics, Pediatric Endocrinology, Endocrinology, Internal Medicine, Medical Genetics, or related discipline.

• Experience working within multidisciplinary clinical development teams, including structured 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 quality standards.

• Excellent communication and leadership skills.

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

Preferred

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

• Industry experience within 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 Lead or Study Team Leadership experience, with demonstrated ability to apply disciplined study oversight, protocol development, and document review practices.

Salary Range: $265k to $320k

About Angitia

Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused 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 the team'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 core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built its headquarters in Westlake 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. The 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 vibrant group.

Learn more at .

Benefits:

• Medical, dental, and vision coverage for employees and their eligible dependents

• 401(K) Retirement Plan with Company match

• Company paid Long Term Disability Coverage

• Company-paid life Insurance & AD&D Coverage

• Voluntary Life Insurance & AD&D Coverage

• Employee Assistance Program (EAP)

• Company-paid Holidays

• Vacation

• Paid Sick Leave

• Telecommunication Monthly Stipend

• Work-From-Home Equipment Reimbursement

Originally posted on Himalayas