Associate Director, Clinical Development

Job Summary

The Associate Director, Clinical Development will support clinical trial related activities for Brelovitug, a key asset in Phase 3, on a cross-functional team of internal and external experts, investigators, and government agencies. Responsibilities include drafting clinical trial and program-level documents, protocol development, study startup, recruitment, ongoing clinical development management, and closeout.

Job Functions/Responsibilities

• Responsible for drafting key clinical trial and program-level documents in collaboration with Clinical Operations, Biostats, Medical Writing, and CROs
• Supports clinical aspects of study startup, execution, and close-out in collaboration with Clinical Operations, Data Management, and CRO
• Supports monitoring of efficacy and safety data received from clinical trials
• Supports preparation of clinical summaries for drug applications
• Supports preparation of scientific/medical questions from regulatory agencies
• Supports analysis and drafting of clinical trial and scientific publications
• Supports planning, conduct, and follow-up of external clinical development- or study-related meetings
• Responsible for clinical aspects of the Trial Master File (TMF)
• Supports the running and operational aspects of the Clinical Development team including meeting support, inspection readiness, and organizational support

Qualifications

• Education/Experience: Bachelor’s Degree and/or advanced degree in a scientific discipline; PhD or PharmD preferred; 3+ years of experience in the pharmaceutical industry, including 2+ years in Clinical Development teams; Manage several clinical trials with multidisciplinary trial teams; Experience in working with CROs; Medical/scientific expertise appropriate to clinical program; Demonstrates ability to establish strong scientific partnership with key investigators
• Knowledge, Skills and Abilities: Demonstrated accountability for delivery on clinical studies; Demonstrates excellent scientific writing skills; Experience with basic statistical principles and techniques of data analysis, interpretation, and clinical relevance; Strong experience in clinical data review and interpretation; Ability to execute in a fast-paced environment; Detail oriented with exceptional organizational skills; Effective communicator with strong verbal and written skills; Ability to identify issues, analyze situations, and provide effective solutions; Solid understanding of the clinical development process

Company Information

Mirim Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.

Mirim Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws.

Mirim Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.