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Associate Clinical Project Manager

8+ years
$98,000 – $196,000 annually
10 July 29, 2025
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

 

Associate Clinical Project Manager – Abbott (Alameda, CA)

Job Summary:
Abbott, a global healthcare leader, is seeking an Associate Clinical Project Manager in Alameda, California, to support and lead the execution of critical clinical trials. This on-site role is ideal for professionals with strong experience in clinical research and project management who are looking to work with cutting-edge medical technologies in a regulated and innovative environment. With competitive compensation ranging from $98,000 to $196,000, this role offers growth, responsibility, and the opportunity to make a lasting impact in the healthcare industry.


Key Responsibilities:

  • Manage and support execution of assigned clinical projects and ensure ongoing audit readiness

  • Conduct and support clinical visits to ensure proper site monitoring and protocol adherence

  • Lead communication with core teams and contribute clinical input to product development

  • Monitor project reports for trends, accuracy, and budgeting metrics

  • Ensure safety signals and adverse event trends are identified and addressed

  • Support planning for post-project activities and market launches

  • Negotiate contracts and budgets with research sites and maintain financial oversight

  • Coordinate with legal and clinical teams to ensure regulatory compliance and documentation

  • Review and approve invoices; track clinical study accruals and budget adherence

  • Implement corrective actions for compliance deviations


Required Skills & Qualifications:

  • Bachelor’s degree in Biological Sciences, Engineering, or related field (Advanced degree preferred)

  • 8+ years in clinical research or laboratory environment

  • 1–3 years managing clinical projects in a cross-functional setting

  • Experience with medical device clinical trials preferred

  • Proficient in GCP, FDA, and ISO regulatory requirements

  • Strong verbal and written communication skills

  • Excellent organizational, problem-solving, and data interpretation skills

  • Proficient in Microsoft Office Suite and clinical applications

  • Willingness to travel up to 20%


Perks & Benefits:

  • Competitive salary: $98,000 – $196,000 annually

  • Career advancement in a global healthcare company

  • Excellent medical, dental, and vision coverage

  • Retirement savings plan with strong employer contribution

  • Tuition reimbursement and continuing education support

  • Recognized as a top employer globally for diversity and innovation


Company Overview:

Abbott is a global healthcare leader with over 114,000 employees operating in 160+ countries. Our mission is to help people live more fully through life-changing technologies in diagnostics, medical devices, nutrition, and branded generic medicines. We are committed to clinical innovation, scientific excellence, and advancing global health.


Work Mode: On-site (Alameda, California)


Ready to Take the Next Step?

If you have a passion for clinical excellence and want to help bring meaningful therapies to market, apply today and join a mission-driven team shaping the future of healthcare.