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Senior Clinical Research Specialist - Nutrition - Columbus, Oh

Abbott
Abbott
5+ years
$66,700.00 – $133,300.00
10 Feb. 5, 2025
Job Description
Job Type: Full Time Education: BA 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

Job Title: Senior Clinical Research Specialist – Nutrition
Location: United States - Ohio - Columbus
Category: Medical and Clinical Affairs


About the Role

Abbott is seeking a Senior Clinical Research Specialist to join the Nutrition division in Columbus, OH. The role involves managing high-priority and complex clinical trials from protocol development to study closeout. You'll collaborate with cross-functional teams to meet business objectives while ensuring compliance with Abbott policies and regulations.


Key Responsibilities

  • Clinical Trial Execution: Manage all aspects of assigned clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards.
  • Protocol Review: Review and contribute to the development of protocols, Case Report Forms (CRFs), enrollment procedures, randomization, and blinding processes.
  • Clinical Trial Management: Handle study activities in eTMF and Clinical Trial Management Systems (CTMS), including document tracking, shipments, product accountability, and supply management.
  • Stakeholder Interaction: Represent Abbott in interactions with external stakeholders, including physicians and study site personnel.
  • Investigator Sponsored Studies (ISS): Manage the lifecycle of ISS, including submission, review, and approval, ensuring compliance with internal processes and regulations.

Skills and Qualifications

  • Education: BA in health profession or scientific related field preferred.
  • Experience:
    • 5+ years in the clinical research industry.
    • Proficiency with clinical trial management systems, eTMF, and payments systems.
    • Understanding of Good Clinical Practice (GCP) and industry standards.
  • Skills:
    • Strong organizational, communication, and interpersonal skills.
    • Ability to work under pressure and take initiative on unfamiliar tasks.
    • Team-oriented with high energy and a strong desire to achieve results.

Benefits

  • Career Growth: Opportunities for professional development with a global leader in healthcare.
  • Healthcare Benefits: Free medical coverage in the next calendar year for employees in the Health Investment Plan (HIP).
  • Retirement & Savings: Excellent retirement savings plan with high employer contributions.
  • Education Support: Tuition reimbursement, student debt programs, and educational benefits for pursuing a bachelor's degree.
  • Work Environment: Recognized as one of the best places to work for diversity, working mothers, and women in leadership.