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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: Pune, India

Experience Required: 1 – 2 Years

Job Description:

We are looking for a Clinical Research Associate-I (CRA-I) to join our team in Pune on a full-time basis. The ideal candidate will have 1-2 years of experience in clinical research and will be responsible for assisting with the execution and monitoring of clinical trials in accordance with regulatory guidelines, protocols, and industry standards.

Key Responsibilities:

  • Assist in site selection, initiation, monitoring, and close-out visits for clinical trials.
  • Ensure adherence to study protocols, ICH-GCP, and local regulatory requirements.
  • Review and verify clinical trial documentation, including source documents and case report forms (CRFs), ensuring accuracy and completeness.
  • Support the recruitment, enrollment, and retention of study participants.
  • Monitor site performance and provide guidance to ensure study timelines are met.
  • Collaborate with investigators and study teams to resolve any issues related to the trial.
  • Maintain accurate and up-to-date records for all clinical trial activities.
  • Assist in preparation and submission of study reports and other related documents.
  • Stay informed about current regulatory guidelines and industry trends to ensure compliance.

Qualifications:

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

This position is an excellent opportunity for a Clinical Research Associate-I to gain hands-on experience in clinical trials and further develop your career in clinical research. If you are motivated and ready to contribute to a fast-paced, innovative environment, we encourage you to apply. 

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