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Clinical Project Manager Ii - Oncology & Vendor Mgt Experience Required (Sponsor Dedicated/ Foster City, Ca Or Remote)

3+ years
$85,500 - $175,700
10 Dec. 1, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

The Clinical Project Manager II - Oncology & Vendor Management role at Syneos Health is a key position within their Oncology therapeutic area. The role is home-based in the United States (preferably near Foster City, CA), with the requirement to be in the office 2-3 days a week. This position involves overseeing global clinical trials, managing vendors, and ensuring that projects are delivered on time, within budget, and in compliance with regulatory standards.


Position Overview

  • Location: Home-Based, US (preferably Foster City, CA)
  • Job ID: 24006433
  • Updated: November 25, 2024

This Sponsor Dedicated role focuses on managing clinical research studies from start-up to close-out, with a strong emphasis on oncology expertise. The Clinical Project Manager II will also be responsible for managing vendors, timelines, and budgets while ensuring quality and compliance across all clinical trial operations.


Key Responsibilities

  1. Project Leadership and Delivery:

    • Lead interdisciplinary clinical research studies, ensuring compliance with GCP, SOPs, and regulatory requirements.
    • Act as the primary liaison between the company and the customer for study execution.
    • Oversee project team activities to ensure timelines, quality, and budgets are met.
    • Manage the financial performance of the project and proactively identify and resolve issues.
  2. Documentation and Reporting:

    • Ensure quality and completeness of the Trial Master File (TMF) for assigned projects.
    • Maintain study information on relevant databases and ensure inspection readiness.
    • Prepare and present internal and external meeting reports.
  3. Risk Management:

    • Develop and implement contingency plans and risk mitigation strategies.
    • Oversee the development of project plans and ensure adherence to timelines and deliverables.
  4. Business Development:

    • Cultivate strong relationships with clients to generate new business opportunities.
    • Participate in bid defense meetings and support the development of business proposals.
  5. Management and Oversight:

    • Manage and mentor project management and clinical monitoring staff as needed.
    • Support the training and development of junior team members.

Qualifications

  • Education:

    • Bachelor’s degree or equivalent in life sciences, medicine, pharmacy, nursing, or a related field.
  • Experience:

    • Minimum 3 years of experience in clinical project management or study management within a CRO or pharma setting.
    • Strong background in oncology is required.
    • Experience in vendor management, timeline oversight, and budget management.
  • Skills:

    • In-depth knowledge of Good Clinical Practice (GCP) and ICH guidelines.
    • Strong organizational skills, ability to work independently, and excellent communication skills.
    • Ability to travel approximately 25% as required.

Why Syneos Health?

Syneos Health is committed to fostering a diverse and inclusive work environment. They offer career development opportunities, training, and a culture where employees can authentically be themselves. Syneos Health’s Total Self Culture is at the core of their operations, driving them to create an environment that nurtures innovation and collaboration.


Additional Information

  • Salary Range:
    The annual base salary for this role ranges from $85,500 to $175,700, depending on experience, skills, and qualifications.

  • Benefits:

    • Health benefits including medical, dental, and vision.
    • 401k match, Employee Stock Purchase Plan.
    • Flexible paid time off (PTO) and sick time.

This position provides an exciting opportunity to lead clinical research in the oncology field while working with a globally recognized team.