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Senior Director, Clinical Research

10+ years
Not Disclosed
10 June 10, 2025
Job Description
Job Type: Full Time Education: PhD, PharmD, Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Senior Director, Clinical Research – ArriVent | San Francisco Bay Area

Job Summary

ArriVent, a clinical-stage biopharmaceutical company in the San Francisco Bay Area, seeks a Senior Director of Clinical Research to lead the design, development, and execution of oncology-focused clinical trials. The ideal candidate will oversee clinical programs, mentor a team of Clinical Scientists, and play a critical role in regulatory submissions including INDs, NDAs, and safety reports. This full-time, on-site leadership role offers an opportunity to impact the future of solid tumor oncology drug development in a dynamic biotech environment.

Salary Range: Not specified


Key Responsibilities

  • Lead the creation of clinical development deliverables: protocols, CSRs, Investigator’s Brochures (IBs), and regulatory documents.

  • Oversee development of regulatory filings (INDs, NDAs, Safety Reports) and handle responses to health authority queries.

  • Direct and monitor ongoing clinical trials to ensure protocol compliance and assess study progress.

  • Analyze data in collaboration with Data Management, Statistics, and Programming teams.

  • Mentor and manage Clinical Scientists, supporting their professional development.

  • Drive process improvements across clinical programs and cross-functional teams to optimize portfolio delivery.


Required Skills & Qualifications

  • PhD, PharmD, or equivalent degree required.

  • 10+ years in clinical development within the biotech/pharmaceutical industry.

  • Proven expertise in solid tumor oncology clinical trials.

  • Experience with authoring protocols, CSRs, IBs, INDs, NDAs, and regulatory response documents.

  • Strong leadership and mentoring abilities.

  • Effective communicator with excellent written and verbal skills.

  • Ability to work autonomously in a small, fast-paced company environment.

  • Collaborative and team-oriented mindset.


Perks & Benefits

  • Competitive compensation package (exact salary not disclosed)

  • Opportunity to lead critical oncology drug development programs

  • Professional growth in a dynamic, science-driven biotech company

  • Work closely with top-tier medical and regulatory experts

  • Contribute to transformative therapies for solid tumor oncology


Company Description

ArriVent is a cutting-edge biopharmaceutical company dedicated to advancing novel oncology therapies. Headquartered in the San Francisco Bay Area, ArriVent’s pipeline focuses on breakthrough treatments designed to address unmet medical needs in cancer care. The company fosters a collaborative, fast-paced environment where scientific excellence drives innovation.


Work Mode

On-site – San Francisco Bay Area


Call to Action

Are you ready to lead the next generation of oncology clinical trials? Apply now to join ArriVent as Senior Director, Clinical Research and shape the future of cancer therapy development.