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1–2 jobs· newest first

Medical Director - Oncology
Lifelancer · Remote, United Kingdom
Remote · Full-time
Senior Executive Director Regulatory Affairs - Advanced Genetic Medicine
Children's Hospital of Philadelphia · Philadelphia, US
$100K–$375KFull-time · Senior

+10K new in the last hour

Medical Director - Oncology

Lifelancer · Posted Nov 6, 2026

Remote, United Kingdom
Remote
Full-time
10+ years

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AI

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Provide medical and scientific oversight for clinical trials, serve as Medical Monitor, support protocol development, safety monitoring, data review, and business development activities for oncology/hematology studies.

Responsibilities

Provide medical and scientific input to clinical research programs
Ensure medical activities comply with GCP
Develop and review study protocols and safety plans
Provide on‑call coverage for protocol queries
Review and analyze safety data and adverse events

Requirements

Medical Degree from an accredited medical school
Nice to have: 3-5 years biopharmaceutical industry experience
Nice to have: Oncology/Hematology specialization
Nice to have: Board Certified/Eligible in Oncology

Skills

Medical oversight Clinical research GCP compliance Protocol development Safety monitoring Data analysis eCRF review IND/SUSAR reporting Statistical and data management collaboration eCRF IND SAE DSMB Statistical software

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Senior Executive Director Regulatory Affairs - Advanced Genetic Medicine

Children's Hospital of Philadelphia · Posted Nov 4, 2026

Philadelphia, Pennsylvania, United States
Full-time · Senior
$100K–$375K per year
12+ years

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Compensation

$100,000.00 - $375,000.00 Annually

Responsibilities

Lead regulatory planning from preclinical development through marketing authorization and lifecycle management for advanced genetic therapies
Provide strategic guidance for INDs, CTAs, BLAs, MAAs, and post-approval activities
Serve as primary regulatory liaison with the FDA and other regulatory agencies for submissions, communications, and inquiries
Coordinate responses to FDA information requests and regulatory submissions
Lead cross-functional teams in preparation for regulatory agency meetings

Requirements

Bachelor's Degree
Master's Degree

Skills

Regulatory Affairs Gene Therapy FDA IND BLA GCP ICH

Quality Assurance

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