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Clinical Trials Manager - I#25-02216

5+ years
Not Disclosed
10 March 21, 2025
Job Description
Job Type: Full Time Education: PharmD/MS/BA/BS/RN 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

Clinical Trials Manager - I#25-02216
Location: Foster City, CA
Type: All On-site

Job Description:

Responsibilities:

  • Participate in multiple Phase 1-4 clinical study teams.

  • Plan and coordinate all operational activities required for the collection, delivery, and analysis of biological specimens within a clinical trial.

  • Provide sample management expertise to the Study Management Teams (SMTs) and Clinical Pharmacology Sub-teams (CPST).

  • Ensure biological samples collected are of good quality and adhere to ethical standards and informed consent guidelines.

  • Act as the primary interface for operational activities between the SMT and laboratory vendors.

  • Manage vendor operations to ensure consistent delivery and quality standards.

  • Evaluate scientific proposals or protocols and budgets for clinical operation feasibility.

  • Identify potential operational challenges and collaborate with senior team members to develop resolution plans.

  • Review and interpret relevant documents, including protocols, informed consents, and other study-related documents.

  • Explain protocol requirements to other team members.

  • Support project priorities within the functional area.

  • Contribute to RFP development and participate in vendor selection.

  • Address functional issues from an organizational perspective.

  • Contribute to or lead special projects.

  • Develop tools and processes to enhance project efficiency and effectiveness.

  • Participate in multiple strategic initiatives under limited supervision.

  • Provide knowledge and expertise on country-specific regulations.

  • Manage project meetings and conference calls with vendors and cross-functional teams.

  • Provide input on study protocols, case report forms, informed consents, study plans, and presentations.

  • Collaborate with Clinical Operations colleagues to resolve operational challenges and ensure study execution remains on track.

  • Ensure compliance with established practices, policies, and regulatory requirements.

Requirements:

  • PharmD: 2+ years of relevant clinical or related experience in life sciences.

  • MS: 3+ years of relevant clinical or related experience in life sciences.

  • BA/BS/RN: 5+ years of relevant clinical or related experience in life sciences.

  • Proficiency in Senior Clinical Trial Management Associate (Senior CTMA) grade 26 requirements.

  • Demonstrated flexibility and adaptability to manage multiple projects.

  • Ability to manage full cycle study management, from start-up to close-out.

  • Advanced knowledge of study management best practices and tools.

  • Thorough understanding of protocol requirements and ability to interpret and communicate effectively.

  • Strong knowledge of FDA, EMA, ICH, and GCP regulations for clinical studies.

  • Familiarity with standard medical/scientific terminology.

  • Experience managing external vendors.

  • Strong communication skills and ability to work in a matrixed environment.

  • Ability to manage and execute multiple tasks effectively.