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Associate Clinical Science Director (Oncology)

3-5 years
Not Disclosed
10 Dec. 9, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Associate Clinical Science Director (Oncology)

Location: Global
Department: Clinical Science | Oncology
Job Type: Full-Time

Position Summary

The Associate Clinical Science Director (Oncology) plays a critical leadership role in designing, planning, and developing clinical evaluation studies focused on solid tumors. This position works closely with cross-functional clinical and project teams to support ongoing oncology programs, develop clinical documents, interpret study results, and provide scientific insights throughout the clinical development lifecycle. The role requires strong oncology clinical study experience and the ability to collaborate across medical, clinical operations, and scientific functions.


Key Responsibilities

  • Design, develop, and initiate study protocols and related documents in alignment with project goals, regulatory standards, GCP, and good medical practice.

  • Conduct comprehensive literature reviews to support clinical strategy and study planning.

  • Partner with the medical monitor to enable effective interaction with clinical sites and key oncology investigators.

  • Collaborate with Clinical Operations and cross-functional teams to develop Informed Consent Forms, Case Report Forms, and CRF instructions.

  • Support preparation of agendas, training materials, and presentations for investigator meetings, site visits, and internal study-related discussions.

  • Participate in internal safety meetings, evaluate potential safety events, and coordinate safety reporting with the medical monitor.

  • Contribute to the review and interpretation of study data in preparation for regulatory submissions, clinical study reports, and close-out documentation.

  • Assist in writing and reviewing abstracts, manuscripts, and other scientific publications.

  • Provide scientific updates, insights on emerging oncology trends, and competitive intelligence.

  • Deliver high-quality scientific presentations to physicians and external stakeholders.

  • Maintain strong clinical and technical expertise within the therapeutic area of oncology.


Supervisory Responsibilities

  • This position does not include supervisory responsibilities.


Education and Experience Requirements

Required Education:

  • Pharm.D., Ph.D., M.D., or equivalent degree with a minimum of five years of relevant experience, OR

  • Equivalent combination of advanced education and industry experience.

Experience Required:

  • Minimum 3–5 years of clinical development experience in biotechnology, pharmaceutical, or a mix of academia and industry.

  • Hands-on experience in oncology clinical studies involving targeted therapies or immunotherapies.

  • Strong understanding of solid tumor oncology research and clinical trial endpoints.


Knowledge, Skills, and Competencies

  • Strong understanding of clinical trial operations, clinical development pathways, and regulatory requirements.

  • Broad knowledge of related disciplines involved in clinical trial execution.

  • Ability to design and implement scientific methods and procedures with attention to quality and compliance.

  • Advanced analytical, scientific writing, and data interpretation skills.

  • Strong presentation, public-speaking, and communication skills.

  • Highly organized, with ability to manage multiple priorities under tight timelines.

  • Ability to apply scientific concepts creatively to solve complex clinical development challenges.

  • Capacity to collaborate across multidisciplinary teams and engage with external experts.


Job Complexity

  • Works on complex clinical and scientific challenges requiring independent judgment and evaluation of diverse factors.

  • Applies professional knowledge to develop solutions aligned with company policies and clinical development standards.

  • Regularly interacts with cross-functional experts and external thought leaders in oncology.


Working Conditions

  • Travel requirement: 10%–25%, depending on study needs and meeting schedules.


Compensation

The base salary range for this position is USD 158,000 – USD 224,500 annually, adjusted based on geographic region, relevant skills, internal equity, and professional experience.

Total Rewards Package Includes:

  • 401(k) with company contributions

  • Comprehensive medical, dental, and vision coverage

  • Life and disability insurance

  • Flexible spending accounts

  • Annual bonus eligibility or sales incentive plan (as applicable)

  • Employee stock purchase program and long-term incentive opportunities

  • 15 days of vacation in the first year

  • 17 paid holidays, including a company-wide winter shutdown

  • Up to 10 paid sick days annually


Disclaimer

This job description outlines the general responsibilities and qualifications for the role. It is not intended to be an exhaustive list of all duties, skills, or requirements that may be assigned.