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Clinical Research Associate-I

1-2 years
Not Disclosed
10 Jan. 23, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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: Clinical Research Associate-I

Location: Boston, USA

Experience Required: 1 – 2 Years

Job Description:

We are seeking a Clinical Research Associate-I (CRA-I) to join our team in Boston. This entry-level role is ideal for candidates with 1 to 2 years of experience in clinical research. The CRA-I will play an integral role in supporting the execution and monitoring of clinical trials, ensuring compliance with study protocols, regulatory guidelines, and industry standards.

Key Responsibilities:

  • Assist in site selection, initiation, monitoring, and close-out visits for clinical trials.
  • Ensure that clinical trials are conducted in compliance with ICH-GCP, local regulatory guidelines, and study protocols.
  • Review study-related documents (source data, CRFs, etc.) for accuracy and completeness.
  • Support sites with patient recruitment, enrollment, and retention efforts.
  • Track and report study progress, ensuring milestones and timelines are met.
  • Collaborate with clinical teams, investigators, and vendors to resolve study-related issues.
  • Maintain up-to-date records and documentation related to clinical trial activities.
  • Assist in the preparation of clinical trial reports and other relevant documentation.
  • Stay informed about regulatory changes and emerging industry best practices.

Qualifications:

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related field.
  • 1-2 years of experience in clinical research or clinical trials.
  • Strong understanding of ICH-GCP and local regulatory requirements.
  • Excellent communication, organizational, and time-management skills.
  • Ability to work independently and as part of a team.
  • Proficient in Microsoft Office Suite and Clinical Trial Management Systems (CTMS).
  • Willingness to travel to clinical sites as needed.

This is a great opportunity for a motivated individual to build their career in clinical research. If you have a passion for the field and want to be part of a dynamic team in a thriving environment, we encourage you to apply.

Send your CV at career@prorelixresearch.com to explore career opportunities with ProRelix Research.