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CLINEXEL Hiring for Medical Writer, QA, CDM, CRA & Admin roles

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Are you passionate about clinical research and healthcare innovation? CLINEXEL, a leading full-service Contract Research Organization (CRO), is expanding its team in Navi Mumbai. With a commitment to quality, compliance, and innovation, CLINEXEL invites motivated professionals to join its growing workforce across multiple roles.

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Whether you are an experienced Medical Writer, Quality Assurance professional, Clinical Data Manager, CRA, or an Office Administrator, this is your chance to thrive in a collaborative and rewarding environment.


📌 Open Positions at CLINEXEL

1️⃣ Medical Writer (Regulatory Documents – Clinical Trials)

Responsibilities:

  • Prepare and review regulatory documents: Study Protocols, ICFs, Clinical Study Reports, Investigator Brochures, and Summary Reports.
  • Work on regulatory submissions for drugs, biologics, CGT, and medical devices.

Qualifications & Experience:

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  • PhD/M.Pharm/B.Pharm
  • 4–10 years of clinical research experience

📍 Location: Navi Mumbai


2️⃣ Sr Manager/Manager – Quality Assurance (Clinical Trials)

Responsibilities:

  • Ensure compliance with ICH-GCP & regulatory standards.
  • Conduct site, vendor, and system audits.
  • Develop SOPs, audit strategies, and training materials.
  • Lead client audits.

Qualifications & Experience:

  • Postgraduate/Graduate in Life Sciences/Pharmacy
  • 6–10 years of relevant clinical trials experience

📍 Location: Navi Mumbai


3️⃣ Sr Executive/Executive – Clinical Data Management (CDM)

Responsibilities:

  • Manage CDM lifecycle activities: from start-up to database lock.
  • Prepare study documents, DMP, eCRFs, reports.
  • Develop DTS, perform UAT, data cleaning, and query resolution.

Qualifications & Experience:

  • Postgraduate/Graduate in Life Sciences/Pharmacy
  • 2–5 years of relevant CDM experience

📍 Location: Navi Mumbai


4️⃣ Sr Clinical Research Associate (Sr CRA)

Responsibilities:

  • Conduct monitoring visits as per protocol, GCP/ICH guidelines, and regulatory requirements.
  • Support project managers in trial management.

Qualifications & Experience:

  • Postgraduate/Graduate in Life Sciences/Pharmacy
  • 4–6 years of trial monitoring experience

📍 Location: Navi Mumbai


5️⃣ Office Administration Staff

Responsibilities:

  • Provide general admin support to staff and management.
  • Manage travel bookings, office supplies, bills, and expenses.
  • Perform ad hoc data entry and coordination tasks.

Qualifications & Experience:

  • Graduate/Postgraduate (preferably Commerce)
  • Minimum 1 year of admin experience, tech-savvy candidates preferred

📍 Location: Navi Mumbai


🎁 Benefits of Working with CLINEXEL

  • Opportunity to work in a full-service CRO with global exposure
  • Competitive salary packages (₹3,00,000 – ₹18,00,000 per annum depending on role & experience)
  • Professional development & continuous training
  • Collaborative & growth-focused work environment

📩 How to Apply

Interested candidates can send their updated CV to:

👉 careers@clinexel-cro.com

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