Instagram
youtube
Facebook

Sr. Scientist Clinical Research

8+ years
$86,700 – $173,300
10 July 4, 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

 

Sr. Scientist Clinical Research – Abbott (Santa Clara, CA / Temecula, CA / New Brighton, MN)

Job Summary:

Abbott, a global leader in medical technologies, is hiring a Sr. Scientist Clinical Research for its Vascular Division. This on-site role is ideal for experienced professionals with strong expertise in clinical trial design, regulatory strategy, and cross-functional collaboration in the medical device space. The role will contribute directly to developing protocols, scientific publications, and global clinical strategies.


Key Responsibilities:

  • Write and revise clinical trial protocols, amendments, study reports, and scientific publications.

  • Collaborate with Regulatory Affairs to support FDA submissions and strategic communications.

  • Provide clinical feedback to cross-functional teams on product development and documentation.

  • Present clinical data at conferences, meetings, and regulatory forums.

  • Interact with teams such as R&D, Sales & Marketing, Clinical Operations, and external CROs.

  • Participate in audits, CAPAs, and quality compliance activities.

  • Mentor junior clinical staff and lead project teams when needed.

  • Stay current on scientific literature and competitive technologies in vascular and interventional therapy.

  • Contribute to root cause analysis and preventive actions for audit findings.


Required Skills & Qualifications:

  • Bachelor’s degree in life sciences, medicine, or related discipline (advanced degree preferred).

  • Minimum 8+ years of experience in clinical research, medical writing, or scientific affairs.

  • Strong understanding of medical device regulations and GCP compliance.

  • Experience with protocol development, clinical trial reporting, and regulatory documentation.

  • Ability to lead cross-functional projects and collaborate with regulatory bodies.

  • Strong presentation, writing, and leadership skills.

  • Prior experience working in a Quality System Environment (QSR).


Perks & Benefits:

  • Base salary range: $86,700 – $173,300 depending on location

  • Free employee medical coverage through HIP PPO plan

  • High employer contribution to 401(k) retirement savings

  • Tuition reimbursement, Freedom 2 Save student loan support, FreeU education benefit

  • Global career development and advancement opportunities

  • Inclusive work environment recognized by Fortune and other major organizations


Company Description:

Abbott is a world-renowned healthcare innovator offering transformative technologies in medical devices, diagnostics, branded generics, and nutritionals. With a strong focus on advancing science and delivering patient-centric solutions, Abbott empowers professionals in over 160 countries to shape the future of health.


Work Mode:

On-site – Preferred location: Santa Clara, CA; also available in Temecula, CA and New Brighton, MN


Call to Action:

Advance your career by joining a globally respected leader in clinical research and medical device innovation. Apply now to become a Sr. Scientist Clinical Research at Abbott and contribute to breakthrough science improving lives around the world.