Brillex Clinical Hiring Medical Writer, Medical Monitor, Principal Investigator, Subject Recruiter

BPharm MPharm Clinical Research Jobs Brillex Ahmedabad

B.Pharm, M.Pharm, MD candidates apply for multiple CRO roles at Brillex Clinical Research Ahmedabad (1–8 yrs experience).

Brillex Clinical Research Pvt. Ltd. is hiring for multiple roles in clinical research, offering excellent opportunities for professionals in pharmacology, clinical trials, and medical writing. Based in Ahmedabad, this hiring drive targets candidates with 1 to 8 years of experience who want to build or advance their careers in CRO (Contract Research Organization) environments.

With the rapid growth of clinical research jobs, CRO jobs in India, and medical writing careers, these openings are highly relevant for candidates looking to work in late-phase clinical trials, BA/BE studies, and regulatory medical documentation. High CPC keywords such as clinical research jobs, medical writing jobs, CRO jobs, clinical trial jobs, and pharmacology careers are strategically integrated to boost search visibility and AdSense revenue.

Company Overview

Brillex Clinical Research Pvt. Ltd. is a growing Contract Research Organization (CRO) specializing in clinical trials, BA/BE studies, and regulatory documentation. The company supports pharmaceutical and biotech companies in conducting compliant and efficient clinical research studies.

With a focus on quality, ethics, and regulatory compliance, Brillex plays a critical role in advancing drug development and ensuring safe and effective therapies reach the market. The organization provides professionals with exposure to global clinical trial standards and regulatory frameworks.

Job Role & Responsibilities

Medical / Protocol Writer (Late Phase)

• Prepare clinical trial protocols and study documents for late-phase trials
• Develop regulatory-compliant medical writing content
• Collaborate with clinical and regulatory teams
• Ensure accuracy and adherence to global clinical guidelines

Medical Monitor – Clinical Trial

• Provide medical oversight for clinical trials
• Review safety data and clinical outcomes
• Support feasibility assessments and protocol development
• Ensure compliance with clinical and regulatory standards

Principal Investigator (BA/BE Studies)

• Conduct and supervise bioavailability and bioequivalence studies
• Ensure ethical conduct and regulatory compliance of trials
• Oversee subject safety and study execution
• Maintain accurate clinical documentation

Volunteer / Subject Recruiter (Early Phase Clinic)

• Identify and recruit eligible subjects for clinical trials
• Maintain subject databases and recruitment pipelines
• Coordinate with clinical teams for study participation
• Ensure compliance with recruitment guidelines and protocols

These roles are essential in ensuring clinical trial accuracy, patient safety, and regulatory compliance in drug development processes.

Eligibility / Qualifications

Educational Qualification

• B.Pharm, M.Pharm, MD (Pharmacology)
• Relevant Courses: Pharmacology, Clinical Research, Pharmaceutics, Biotechnology, Life Sciences, Medical Writing, Regulatory Affairs

Experience Required

• Medical Writer: 1–3 years
• Medical Monitor: 2–3 years
• Principal Investigator: 2–4 years
• Subject Recruiter: 2–8 years

Key Skills

• Knowledge of clinical trials and CRO operations
• Experience in medical writing and protocol development
• Understanding of GCP (Good Clinical Practice) guidelines
• Strong communication and documentation skills
• Ability to manage clinical study processes

Location & Salary

• Location: Ahmedabad (Gujarat)
• Salary: As per industry standards (based on experience and role)

Application Process

Interested candidates can apply using the details below:

• Email: hr@brillexcro.com
• Website: https://www.brillexcro.com/
• Address: 602, Ariane Legacy, Near Maharaj Hotel, SG Highway, Adalaj, Gandhinagar, Gujarat, India

Candidates are advised to mention the applied position clearly in the subject line.

Why This Opportunity Stands Out

• Work in a growing CRO with exposure to clinical trials and drug development
• Opportunities across multiple clinical research roles
• Hands-on experience in late-phase trials and BA/BE studies
• Strong career growth in clinical research and pharmacology domains

FAQs

Who can apply for Brillex CRO jobs?

Candidates with B.Pharm, M.Pharm, or MD (Pharmacology) qualifications can apply depending on the role.

What is the experience required?

Experience ranges from 1 to 8 years depending on the position.

What roles are available?

Medical Writer, Medical Monitor, Principal Investigator, and Subject Recruiter roles are available.

Where is the job location?

The positions are based in Ahmedabad, Gujarat.

How can I apply?

You can send your resume to hr@brillexcro.com.

Additional SEO Titles

• Brillex CRO Hiring Clinical Research Professionals in Ahmedabad
• Medical Writing and Clinical Trial Jobs for Pharma Candidates
• CRO Jobs in India for BPharm MPharm MD Pharmacology

Summary Table

Category	Details
Company	Brillex Clinical Research Pvt. Ltd.
Vacancies	Medical Writer, Medical Monitor, Principal Investigator, Subject Recruiter
Required Education	B.Pharm, M.Pharm, MD (Pharmacology, Clinical Research, Biotechnology, Life Sciences)
Experience	1–8 Years