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Brillex Clinical Research Hiring For Medical Writer, Medical Monitor, Principal Investigator, Screening Coordinator

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Brillex Clinical Research Pvt. Ltd., a fast-growing CRO in Gujarat, is hiring skilled professionals for its late-phase clinical research and BA/BE studies. If you’re looking to build a strong career in clinical research jobs in India, this is an excellent opportunity to join a reputable organization with consistent growth, advanced facilities, and an ethical research ecosystem.

Below are the open positions at the Brillex Ahmedabad location.


Open Positions at Brillex Clinical Research Pvt. Ltd.

1. Medical/Protocol Writer (Late Phase)

Location: Ahmedabad
Qualification: B.Pharm / M.Pharm
Experience: 1–3 years (late-phase clinical trials)

Key Responsibilities

  • Prepare study protocols, CSRs, IBs, and regulatory documents
  • Ensure compliance with ICH-GCP and late-phase trial guidelines
  • Collaborate with clinical operations and biostatistics teams
  • Conduct literature reviews and prepare scientific content

Qualifications

  • Pharma background with strong scientific writing skills
  • Experience in late-phase research documentation

2. Medical Monitor

Location: Ahmedabad
Qualification: M.D. (Pharmacology)
Experience: 2–3 years (late-phase MM, feasibility evaluations, protocol writing)

Key Responsibilities

  • Oversee medical aspects of clinical trials
  • Provide safety monitoring and medical review
  • Support feasibility assessments and develop study protocols
  • Ensure subject safety and regulatory compliance

Qualifications

  • MD Pharmacology with clinical monitoring experience
  • Strong understanding of safety reporting and trial governance

3. Principal Investigator (BA/BE Studies)

Location: Ahmedabad
Qualification: M.D. (Pharmacology)
Experience: 2–4 years in BA/BE studies

Key Responsibilities

  • Lead BA/BE studies as per regulatory norms
  • Oversee subject enrollment, dosing, and sample collection
  • Ensure adherence to SOPs, GCP, and ethical standards
  • Supervise clinical research staff and documentation

Qualifications

  • Experience leading or supporting BA/BE studies
  • Strong decision-making and subject safety oversight

4. Screening Coordinator

Location: Ahmedabad
Qualification: Any Graduate
Experience: 2–5 years (CRO screening & recruitment)

Key Responsibilities

  • Coordinate subject screening and recruitment
  • Manage visit schedules and documentation
  • Maintain screening logs and ensure protocol compliance
  • Support clinical team during pre-study procedures

Qualifications

  • Prior CRO experience is mandatory
  • Strong organizational and communication skills

Why Work at Brillex Clinical Research?

  • Competitive salary (₹4–12 LPA depending on role)
  • Opportunity to work on leading clinical research programs
  • Exposure to advanced CRO workflows and regulatory standards
  • Skill-oriented career development and team mentorship
  • Ethical and transparent work culture

How to Apply

Interested candidates can send their updated CV to:
📧 hr@brillexcro.com

Office Address:
Brillex Clinical Research Pvt. Ltd.,
602, Ariane Legacy, Near Maharaj Hotel,
SG Highway, Adalaj, Gandhinagar, Gujarat, 382421

Brillex Clinical Research Hiring For Medical Writer, Medical Monitor, Principal Investigator, Screening Coordinator

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