Sanofi Hiring Content Editor – Omnichannel in Hyderabad | Pharma Digital Marketing Job 2026 (Sanofi Hiring Content Editor – Omnichannel in Hyderabad) If you are a Life Sciences or Pharmacy professional with experience in medico-marketing content and pharmaceutical digital campaigns, here is a premium opportunity from one of the world’s leading pharmaceutical companies. Sanofi is inviting applications for the position of Content Editor – Omnichannel at its Hyderabad Hub. This is a permanent, full-time pharma digital marketing job designed for professionals with 2–4 years of experience in Omnichannel campaign execution, SEO-optimized healthcare content, and MLR-compliant scientific communication. With pharmaceutical companies increasingly investing in AI-enabled content frameworks and global go-to-market transformation strategies, this role offers strong career growth in the pharma marketing and digital transformation domain. Introduction The pharmaceutical industry is rapidly s...
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"Brillex Clinical Research Pvt. Ltd. Hiring for Multiple Clinical Research Positions in Ahmedabad | CRO Jobs 2026"
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Brillex Clinical Research Pvt. Ltd. Hiring Multiple Clinical Research Professionals in Ahmedabad
(Brillex Clinical Research Pvt. Ltd. Hiring)
Introduction
Ahmedabad is rapidly emerging as a major hub for clinical research and CRO operations in India. Brillex Clinical Research Pvt. Ltd. has announced multiple openings for experienced professionals in late-phase clinical trials, BA/BE studies, medical writing, bioanalytical research, and clinical monitoring.
This hiring drive offers excellent opportunities for B.Pharm, M.Pharm, M.D. (Pharmacology), and Life Sciences graduates who are looking to grow their careers in clinical research jobs in Gujarat. Candidates with experience in protocol writing, medical monitoring, GCP compliance, and bioanalytical operations should strongly consider applying.
If you are targeting CRO jobs in Ahmedabad in 2026, this opportunity provides exposure to regulated environments, late-phase trials, and BA/BE studies.
About The Company – Brillex Clinical Research Pvt. Ltd.
Brillex Clinical Research Pvt. Ltd. is a Gujarat-based Clinical Research Organization (CRO) engaged in conducting late-phase clinical trials, BA/BE studies, and bioanalytical research services. The company operates under regulated standards, ensuring compliance with ICH-GCP guidelines and applicable regulatory frameworks.
Brillex CRO is expanding its operations, creating strong demand for skilled professionals in medical writing, clinical monitoring, and pharmacology domains.
Job Overview Summary
Brillex Clinical Research is recruiting for six different positions across medical writing, clinical monitoring, bioanalytical research, and business development. These roles are designed for professionals with 1–7 years of experience in clinical research and pharmaceutical operations.
The openings focus on late-phase clinical trial documentation, medical oversight, BA/BE study supervision, bioanalytical testing, and site monitoring activities. This hiring initiative reflects the company’s expansion in regulated clinical research operations.
Vacancy Details (Official)
1️⃣ Medical / Protocol Writer (Late Phase)
Qualification: B.Pharm / M.Pharm Experience: 1–3 years Location: Ahmedabad
2️⃣ Medical Monitor – Clinical Trials
Qualification: M.D. (Pharmacology) Experience: 2–3 years Location: Ahmedabad
3️⃣ Principal Investigator (BA/BE Studies)
Qualification: M.D. (Pharmacology) Experience: 2–4 years Location: Ahmedabad
Qualification: B.Pharm / Any Science Graduate Experience: 0–5 years Location: Ahmedabad
6️⃣ CRA – Clinical Trial
Qualification: B.Pharm / Any Science Graduate Experience: 2–7 years Location: Ahmedabad
Responsibility Explanation
Each role has distinct responsibilities within the CRO structure:
Medical / Protocol Writer
Responsible for drafting late-phase clinical study protocols, Investigator Brochures, and Clinical Study Reports (CSR). Ensures ICH-GCP compliance and collaborates with cross-functional teams.
Medical Monitor
Provides medical oversight for clinical trials, evaluates safety data, performs feasibility assessments, and ensures subject protection and regulatory compliance.
Principal Investigator (BA/BE)
Supervises BA/BE clinical studies, ensures protocol adherence, oversees subject safety, and maintains regulatory documentation readiness for audits.
Research Associate – Bioanalytical
Handles sample analysis, method validation, calibration procedures, GLP compliance, and laboratory documentation in bioanalytical departments.
BD Support Executive
Supports business development activities, assists in proposal preparation, conducts market research, and coordinates with clients.
CRA – Clinical Trial
Performs site monitoring visits, ensures GCP compliance, verifies CRF data, and coordinates with investigators.
Eligibility (Official)
Qualifications vary by role:
B.Pharm / M.Pharm
M.D. (Pharmacology)
M.Sc. (Bioanalytical roles)
Any Science Graduate (CRA / BD roles)
Experience Requirement: 0–7 years, depending on position
Location: Ahmedabad, Gujarat
Skills Required
Candidates should possess:
Strong knowledge of ICH-GCP guidelines
Experience in clinical trial documentation
Protocol writing and regulatory documentation skills
Analytical skills for bioanalytical testing
Safety monitoring expertise (for medical roles)
Site monitoring and data verification skills (for CRA)
Communication and coordination abilities
Understanding of BA/BE regulatory standards
GLP and GMP awareness
Salary Estimate
Based on CRO industry standards in Ahmedabad:
Medical Writer: ₹4.5 – ₹7 LPA
CRA: ₹5 – ₹9 LPA
Research Associate (Bioanalytical): ₹4 – ₹8 LPA
Principal Investigator: ₹10 – ₹18 LPA
Medical Monitor: ₹12 – ₹20 LPA
BD Executive: ₹3 – ₹6 LPA
Final salary depends on experience, interview performance, and regulatory exposure.
Interview Details (Official)
Interview details have not been publicly disclosed. Shortlisted candidates will be contacted by HR for technical and HR rounds. The selection process may include:
Technical Interview
Clinical knowledge assessment
HR discussion
Required Documents
Candidates should prepare:
Updated Resume
Educational Certificates
Experience Letters
GCP Training Certificate (if available)
Salary Slips (if experienced)
ID Proof
Passport-size Photograph
Job Location
602, Ariane Legacy, Near Maharaj Hotel, SG Highway, Adalaj, Gandhinagar, Gujarat, India
How to Apply
Interested candidates can share their updated CV at:
Early application is recommended due to limited openings.
FAQs
Q1. Are freshers eligible?
Yes, BD Support Executive allows 0–5 years of experience.
Q2. Is an M.D. mandatory for a Medical Monitor?
Yes, an M.D. (Pharmacology) qualification is required.
Q3. Are these permanent roles?
Yes, full-time CRO positions in Ahmedabad.
Q4. Is BA/BE experience necessary for the PI role?
Yes, 2–4 years of experience in BA/BE studies is required.
Q5. What is the career growth in CRO?
Professionals can grow into Senior CRA, Clinical Project Manager, Regulatory Lead, or Medical Director roles.
Final Conclusion
Brillex Clinical Research Pvt. Ltd. is expanding its clinical research operations in Gujarat and offering strong career opportunities across medical writing, medical monitoring, clinical trial management, and bioanalytical research.
For professionals seeking CRO jobs in Ahmedabad, especially in late-phase clinical trials and BA/BE studies, this hiring drive provides valuable exposure to regulatory-compliant environments. With increasing demand for skilled clinical research professionals in India, joining a growing CRO like Brillex can significantly enhance long-term career prospects.
Candidates meeting the eligibility criteria should apply promptly.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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