Clinical Research Associates

Role & Responsibilities

• Assist in reviewing clinical study protocols, ICFs and trial-related documents

• Identify protocol deviations, inconsistencies and missing data

• Maintain documentation as per SOPs, GCP and regulatory guidelines

• Conduct literature searches using PubMed, Google Scholar and other databases

• Summarize clinical, safety and therapeutic literature

• Support preparation of literature reviews and study summaries

• Assist in clinical trial monitoring activities under supervision

• Review CRFs, essential documents and Trial Master File (TMF)

• Track study timelines, compliance and site-level activities

• Coordinate with investigators, clinical sites and internal stakeholders

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Qualification

• B.Pharm / M.Pharm / Life Sciences graduate

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Experience

• 0 to 1 year (Freshers can apply)

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Skills

• Basic knowledge of clinical research and clinical trial processes

• Understanding of GCP, ICH and regulatory guidelines

• Good documentation and attention to detail

• Strong written and verbal communication skills

• Proficiency in MS Word, Excel and PowerPoint

• Ability to perform scientific literature search and summarization

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About the Company

• A growing clinical research organization offering exposure to real-time clinical trials, regulatory documentation, mentorship and long-term career growth in clinical operations and medical writing

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