Medical Director, Late Development, Pdl1v

2-5 years

$226,300 to $377,100.

Remote, USA

10 Jan. 24, 2025

Job Description

Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates 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

Job Title: Medical Director, Late Development, PDL1V
Location: Europe (Any Pfizer Site), United States - California - South San Francisco, United States - Washington – Bothell
Employment Type: Full-time
Posted: 1 Day Ago
Job ID: 4928214

Job Purpose:

The Medical Director in Late Development provides leadership and expertise in clinical trials, overseeing the design, conduct, and analysis of clinical studies. The role involves collaboration with cross-functional teams to ensure the clinical development program meets scientific, ethical, and regulatory standards. The Medical Director also provides medical guidance to clinical operations teams, investigators, and external stakeholders such as health authorities, ethics committees, and patient advocacy groups.

Key Responsibilities:

1. Study-Level Clinical Development Leadership:

Provide clinical leadership across 2-3 study teams, ensuring scientific rigor and alignment with company objectives.
Conduct medical monitoring activities, including eligibility assessments, data review, and safety monitoring.
Lead peer-to-peer interactions with investigators and serve as the point of contact for clinical issues between study teams, investigators, ethics committees, and regulatory authorities.
Lead the development and maintenance of clinical trial and regulatory documents in collaboration with the Clinical Scientist and cross-functional teams.

2. Strategic Guidance, Clinical Insights & Interpretation:

Collaborate with Clinical Scientists to review and interpret clinical data, identifying key findings and implications for stakeholders.
Stay abreast of the latest clinical developments, literature, and guidelines to advise and drive current and future clinical development plans.

Qualifications:

Required:

Medical degree (MD) is required.
2-5 years of industry experience in clinical development.
Demonstrated leadership capabilities, including the ability to influence peers, develop and coach others, and oversee and guide colleagues to achieve business outcomes.

Preferred:

Relevant clinical or industry experience is considered.

Non-Standard Work Schedule, Travel or Environment Requirements:

Ability to travel to international scientific congresses and internal team meetings 3-6 times per year.
Relocation support may be available based on business needs and eligibility.

Work Location:

Hybrid (Remote and On-Site)

Compensation & Benefits:

Annual base salary range: $226,300 to $377,100.
Eligible for Pfizer's Global Performance Plan with a bonus target of 25% of base salary.
Participation in Pfizer’s share-based long-term incentive program.
Comprehensive benefits package including 401(k), paid vacation, holiday and personal days, medical, prescription drug, dental, and vision coverage, and paid caregiver/parental and medical leave.
Learn more at Pfizer Candidate Site – U.S. Benefits.

EEO & Employment Eligibility:

Pfizer is an equal opportunity employer and complies with all applicable national, state, and local laws governing nondiscrimination in employment.
This position requires permanent work authorization in the United States. Pfizer is an E-Verify employer.

Job Category: Medical

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