Clinical Research Executive

8 years

0 Lacs

Posted:4 weeks ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Clinical Research Executive

Clinical Research

Role Overview:

Specialized in pharmaceutical research and competitive intelligence, with expertise in drug development, clinical trial analytics, and regulatory insights — delivering accurate data.

Key Responsibilities:

Conduct secondary research on drugs, mechanisms, targets, and indications; track innovative drug pipelines, regulatory updates, and clinical trials.

Analyze, maintain, and validate pharmaceutical databases with accuracy on key fields such as drug names, MOA, sponsors, molecule types, and trial data.

Monitor developments from regulatory bodies (US FDA, EMA, CDE, etc.), industry reports, patents, and company filings to provide usable and intellectual data.

Prepare weekly/monthly reports, databooks, and dashboards; deliver strategic recommendations on training the team on accurate data capture and address client queries.

Collect and analyze information from trial registries, filtering by condition, intervention, phase, and recruitment status; capture critical study details such as endpoints, design, inclusion/exclusion criteria, and sponsor information.

Identify tool/process gaps, ensure compliance with company guidelines, and support capability building through training and knowledge sharing to enhance team performance.

Key Skills & Competencies

  • Strong knowledge of

    clinical research

    methodologies, GCP, and regulatory requirements.
  • Experience in

    drug safety

    and pharmacovigilance reporting.
  • Excellent organizational, documentation, and project management skills.
  • Strong interpersonal and communication skills to work effectively with internal teams and external stakeholders.

Qualifications & Experience

  • Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
  • 5–8 years of experience in

    clinical research

    and clinical trial management.
  • Hands-on experience in managing clinical trial operations and regulatory submissions.
  • Prior experience working in CROs, pharmaceutical, or biotechnology companies preferred.


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