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Clinical Research Coordinator

1-3 years
$33.63 – $54.11 Hourly Salary
10 Sept. 30, 2024
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

Description

The Clinical Research Coordinator (CRC) plays a key role in the operational management of clinical research activities, overseeing studies from design and setup through to closeout. In this position, you will implement research activities for one or more studies, manage projects, and prioritize tasks to meet critical deadlines. You will ensure adherence to study protocols and relevant regulations, including institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).

Collaboration is essential in this role; you will work closely with the Principal Investigator (PI), ancillary departments, central research teams, sponsors, institutions, and other stakeholders to support all aspects of studies, including compliant conduct, financial management, and personnel support.

Hourly Salary Range: $33.63 – $54.11

Qualifications

Required:

  • Bachelor’s degree or 1-3 years of experience in study coordination or clinical research coordination.
  • Excellent verbal and written communication skills, with the ability to build rapport and collaborative relationships.
  • Strong organizational skills to manage multiple projects and competing deadlines efficiently and cost-effectively.
  • Analytical abilities to identify problems, evaluate options, and implement effective solutions.
  • Flexibility to adapt to changing job demands and priorities, including working outside standard hours to meet research deadlines.
  • Capability to manage tasks assigned by multiple individuals simultaneously.
  • Familiarity with the clinical research regulatory framework and institutional requirements.
  • Proficiency in mathematical skills for preparing clinical research budgets, with a solid understanding of the budgeting process for clinical trials.
  • Knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GCP) for clinical research.
  • Willingness to work in diverse environments and travel to meetings, off-site visits, and conferences as needed.