Brillex Clinical Research Hiring B.Pharm–MD

Clinical Research Hiring | B.Pharm–MD | Ahmedabad

Brillex Clinical Research hiring Medical Writers, Medical Monitors, PI, Screening Coordinators & PMs in Ahmedabad.

Brillex Clinical Research Pvt. Ltd. is expanding its late‑phase clinical operations and inviting skilled professionals to join its Ahmedabad team. These roles are suited for candidates with strong scientific backgrounds and hands-on experience in late‑phase clinical trials, protocol development, monitoring and BA/BE studies.

Company Overview

Brillex Clinical Research Pvt. Ltd. is a full‑service CRO providing end‑to‑end clinical trial support across late‑phase studies, feasibility assessment, BA/BE projects and regulatory documentation. The organisation is known for scientific rigor, data accuracy and adherence to global clinical research standards.

Job Role & Responsibilities

Medical / Protocol Writer (Late Phase)

Qualification: B.Pharm / M.Pharm
Experience: 1–3 years

• Prepare late‑phase clinical trial protocols and related documents.
• Support feasibility assessment and study design drafting.
• Ensure accuracy, regulatory alignment and clarity in medical content.

Medical Monitor (Late Phase)

Qualification: MD (Pharmacology)
Experience: 2–3 years

• Monitor clinical trial conduct and ensure subject safety.
• Provide medical oversight, feasibility assessment and protocol review.
• Guide investigators and study teams on medical queries.

Principal Investigator (PI)

Qualification: MD (Pharmacology)
Experience: 2–4 years in BA/BE studies

• Lead BA/BE studies and ensure protocol compliance.
• Supervise subject dosing, assessment and documentation.
• Support audits, inspections and data review.

Screening Coordinator

Qualification: Any Graduate (Science preferred)
Experience: 2–5 years (CRO experience in screening & subject recruitment)

• Coordinate subject recruitment and screening activities.
• Ensure accurate documentation and eligibility verification.
• Manage subject communication and scheduling.

APM / PM – Late Phase

Qualification: Any Science Graduate
Experience: 7–12 years in late‑phase clinical trials

• Manage project timelines, deliverables and operational activities.
• Coordinate cross‑functional teams and monitor study progress.
• Ensure regulatory compliance, documentation accuracy and audit readiness.

Eligibility / Qualifications

• Scientific qualifications: B.Pharm, M.Pharm, MD (Pharmacology), Science Graduate.
• Relevant CRO or clinical operations experience as per role.
• Strong understanding of ICH‑GCP, regulatory requirements and study documentation.
• Excellent communication and coordination skills.

Relevant Courses: B.Pharm, M.Pharm Pharmacology, MD Pharmacology, B.Sc Life Sciences, PG Diploma in Clinical Research.

Location & Salary

• Location: Ahmedabad, Gujarat.
• Salary: Competitive; aligned to experience and role.

Application Process

Interested candidates can apply by sharing their updated CV at:
hr@brillexcro.com

For more information, visit: https://www.brillexcro.com/

FAQs

1. Are these onsite roles?
Yes, all roles are based in Ahmedabad.

2. Do medical roles require MD Pharmacology?
Medical Monitor and PI positions require MD Pharmacology.

3. Is CRO experience important?
Yes, especially for Screening Coordinator and PM roles.

4. Are freshers eligible?
No. All positions require relevant clinical research experience.

5. Are these late‑phase specific roles?
Yes, the hiring drive targets late‑phase expertise.

Summary Table

Category	Details
Company	Brillex Clinical Research Pvt. Ltd.
Vacancies	Medical Writer, Medical Monitor, PI, Screening Coordinator, APM/PM
Required Education	B.Pharm, M.Pharm, MD Pharmacology, Science Graduate
Experience	1–12 years depending on the role