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Director, Clinical Development

Open 42d posting dated 2 weeks ago

MISSION

Mirum 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.

POSITION SUMMARY

The Director, Clinical Development will be responsible for supporting 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. Activities include but are not limited to drafting key clinical trial and program-level documents, protocol development, support study startup, recruitment, ongoing clinical development management, and closeout as appropriate. Compliance with internal processes, GCP/ICH and regulatory requirements, study and data monitoring, data analysis are required. The Director, Clinical Development operates in collaboration with other functions including internal Safety, Regulatory, Biometrics, and Clinical Operations teams.

JOB FUNCTIONS/RESPONSIBILITIES

  • Responsible for drafting key clinical trial and program-level documents in collaboration with Clinical Operations, Biostats, Medical Writing and the CROs
  • Responsible for clinical aspects of study startup, execution and close-out in close collaboration with Clinical Operations, Data Management and CRO
  • Supports the monitoring of efficacy and safety data received from the clinical trials
  • Supports preparation of clinical summaries for drug applications
  • Supports preparation of scientific/medical questions from regulatory agencies
  • Support the analysis and drafting of clinical trial and scientific publications
  • Supports the planning, conduct and follow-up of external clinical development- or study-related meetings
  • Responsible for clinical aspects of the TMF
  • Support 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
  • Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process
  • Advanced knowledge of the assigned therapy area is desired, with the capability to interpret, discuss and represent trial or program level data.

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.

#LI-HYBRID

Mirum 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.

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

What this application asks

greenhouse

First Name, Last Name, Email, Phone, Resume/CV, Cover Letter, Location

  • Website optional
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  • How did you hear about this opportunity? choose any
  • Are you within a commutable distance to Foster City and willing to commit to a hybrid work schedule with being on site minimum 2 days per week? choose one
  • If you are not local to the Foster City area, are you willing to relocate? choose one
  • Are you legally authorized to work in the US? choose one
  • Will you now or in the future require sponsorship for employment visa status (for example, H-1B, TN, or other work authorization)? choose one
  • By participating in job interviews, you agree to treat all information shared regarding Mirum’s commercial performance, clinical and scientific data, sensitive corporate information, or any information that would reasonably be deemed (or is explicated noted) as confidential, including discussions and physical renderings/documentations, whether verbal or written as confidential. You are expressly prohibited from disclosing any interview information to third parties or other entities without Mirum’s express written consent. Breach of confidentiality may lead to legal ramifications at the determination of Mirum, termination of your application, or termination of employment if an offer is extended. Do you agree? choose one

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