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Clinical Project Manager

5-7 years
Not Disclosed
10 Nov. 19, 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

Clinical Project Manager

Location: United States – California, Alameda
Category: Medical and Clinical Affairs

Company Overview

Abbott is a global healthcare leader dedicated to improving lives through innovative diagnostics, medical devices, nutrition products, and branded generic medicines. With more than 114,000 employees operating in over 160 countries, Abbott drives advancement across every stage of life through its diverse portfolio of life-changing technologies.


Position Overview

The Clinical Project Manager is an individual contributor role responsible for driving complex clinical projects within Abbott’s Medical and Clinical Affairs division. Based in Alameda, California, this role requires advanced knowledge of clinical operations, strong project management capability, and the ability to influence cross-functional teams.

This position also supports leadership by guiding and mentoring junior clinical staff, optimizing processes, and ensuring clinical trials are executed with full compliance to regulatory and quality standards.


Key Responsibilities

  • Plan, develop, and communicate detailed clinical study timelines and deliverables

  • Collaborate with cross-functional teams to ensure project milestones are met on schedule

  • Maintain consistency across clinical trials by aligning study processes and documentation

  • Oversee day-to-day operational activities of clinical studies in accordance with SOPs, GCP, and applicable country regulations

  • Coordinate investigational device release for clinical use and ensure regulatory adherence

  • Develop, refine, and implement Standard Operating Procedures (SOPs) to support team efficiency

  • Train clinical sites and internal staff on clinical procedures when required

  • Ensure adherence to study protocols and resolve operational challenges proactively

  • Monitor study progress, track performance issues, and communicate updates to leadership

  • Identify opportunities for process improvements and support continuous development initiatives

  • Lead or co-lead assigned projects to support organizational goals


Required Qualifications and Experience

  • Associate degree with 5–7 years of relevant industry experience
    (Bachelor’s degree preferred)

  • Strong understanding of clinical research operations, GCP, and regulatory standards

  • Proven ability to manage complex projects and timelines across multiple stakeholders

  • Excellent written and verbal communication skills

  • Ability to travel 25–30% for site visits, training, and project coordination


Compensation

Base Salary Range: USD 86,700 – 173,300
(Range may vary depending on geographic location and experience.)


Why Join Abbott

Abbott offers extensive opportunities for professional development, competitive compensation, and the ability to contribute to impactful clinical programs that shape the future of healthcare. The company is consistently recognized for excellence in workplace culture, diversity, and innovation.