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GSK

Associate Director, Clinical Sciences

GSK

Clinical sciences leader advancing global oncology trials at GSK, a biopharma company developing vaccines and medicines. Leading study design, clinical data review, safety oversight, protocols, and regulatory submissions.

Posted 8/5/2026full-timeUpper Providence • Pennsylvania • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in oncology clinical development, including protocol writing, regulatory compliance, and safety data monitoring. Proven ability to lead cross-functional teams and communicate effectively with diverse stakeholders in the pharmaceutical industry.

Highest-signal resume keywords
Oncology Clinical Development ExperienceProtocol WritingICH/GCP ComplianceClinical Trial Data ReviewRegulatory Submission Documents

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Study ManagementClinical Study ReportsInformed Consent FormsClinical Development StrategyPharmacovigilanceData AnalysisStudy Procedures ManualsRisk/Benefit Decision MakingGlobal Regulatory GuidelinesClinical Development Phases I-IV
Soft Skills
Communication SkillsInfluencing SkillsNegotiation SkillsLeadership SkillsProblem-Solving Support
Certifications & Qualifications
Bachelor’s Degree in Life SciencesAdvanced Degree (MS, PharmD, PhD) Preferred
Industry Keywords
Pharmaceutical IndustryBiotechnology IndustryContract Research OrganizationsImmuno-OncologyClinical Trials

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Serve as a clinical sciences leader on global oncology studies and contribute to program-level activities
  • Lead delivery of study strategy and design and understand analysis and interpretation of data throughout study conduct
  • Lead ongoing clinical data review and medical review of clinical trial data
  • Own end-to-end writing of protocols from protocol concept through final study report
  • Contribute to informed consent forms and other study-related documents
  • Review and enhance project-level clinical development plans
  • Support regulatory interactions, briefing documents, presentations, questions, and responses
  • Ensure compliance with ICH/GCP guidelines, applicable laws and regulations, and GSK SOPs
  • Contribute to end-to-end clinical development strategy
  • Review and monitor safety data with pharmacovigilance
  • Participate in blinded review of data packages for IDMCs
  • Make risk/benefit decisions and take actions to mitigate risks
  • Collaborate with oncology staff across global functions and cultivate relationships among study/project teams
  • Provide training, education, onboarding, and problem-solving support for clinical trials
  • Provide study-level leadership and accountability for safety and regulatory reporting
  • Drive or contribute to clinical components of investigator brochures and regulatory submission documents
  • Serve as a product, protocol, and project subject matter expert
  • Work with external experts to develop abstracts, manuscripts, and study design presentations

Requirements

What you’ll need
  • Bachelor’s degree in life sciences or related discipline
  • 3+ years of experience in the pharmaceutical/biotechnology industry or related clinical experience
  • Experience in a pharmaceutical industry or CRO environment in the clinical development process
  • Oncology clinical development experience, particularly immuno-oncology
  • In-depth experience with study management, global regulatory guidelines, and ICH/GCP
  • Experience developing and writing study protocols, study procedures manuals, informed consent forms, and clinical study reports
  • Experience working with investigators, site staff, external experts, Contract Research Organizations, and vendors
  • Advanced degree (MS, PharmD, PhD) or equivalent clinical research experience is preferred
  • Clinical development experience across all phases of development (I-IV) is preferred
  • Highly developed communication skills appropriate to the target audience
  • Proven expertise proactively identifying issues affecting clinical programs and contributing to cross-functional solutions
  • Excellent influencing and negotiation skills
  • Excellent leadership skills

Benefits

Comp & perks
  • Comprehensive benefits program for US employees
  • Equal Opportunity Employer
  • Accommodation or other assistance available for applicants
  • Opportunities for growth and career development
  • Wellbeing support
  • Inclusive and welcoming workplace culture