Statistical Programmer Job 2026 in Ahmedabad | SAS & CDISC Jobs at Veeda CR (Statistical Programmer Job 2026 in Ahmedabad) Introduction If you are planning to build a career in clinical data science, SAS programming, or biostatistics, this Statistical Programmer job at Veeda Clinical Research (Veeda CR) in Ahmedabad is an excellent opportunity. With the increasing demand for professionals skilled in clinical data management and regulatory standards, this role provides a strong foundation in pharmaceutical data science and clinical research. Looking for the best multivitamin? Here is the top recommendation: 👉 HealthKart Multivitamin – Best for Daily Energy 👉 Buy Now on Amazon (Best Price) About The Company Veeda Clinical Research (Veeda CR) is a well-established Clinical Research Organization (CRO) headquartered in Ahmedabad, India. Founded in 2004, the company has built a strong reputation in bioequivalence studies, clinical trials, and data management services. Veeda...
Get link
Facebook
X
Pinterest
Email
Other Apps
Pharma Duniya is a trusted platform providing the latest pharma job updates, walk-in interviews, clinical research openings, and pharmacy career guidance.
All job information is collected from official company websites and public sources.
We do not charge any fees and are not official recruiters.
"Brillex Clinical Research Pvt. Ltd. Hiring for Multiple Clinical Research Positions in Ahmedabad | CRO Jobs 2026"
Get link
Facebook
X
Pinterest
Email
Other Apps
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.
📄Resume Getting Rejected Again & Again?
👉 Not getting interview calls?
Most pharmaceutical job applications fail due to poorly formatted or non-ATS-friendly resumes.
👉 Get your Pharma Resume professionally written by experts:
Recommended Pharma Career & Job Updates (Must Read)
If you are preparing for pharma job interviews or actively searching for the latest QA, QC, Pharmacovigilance jobs and walk-in interviews, don’t miss these important and student-friendly career resources from Pharma Duniya 👇
"Macleods Pharma Walk-In for Freshers: Production API, QC Micro, QC, QA Jobs⚡💖"
📢 Stay Updated with Latest Pharma Jobs & Walk-In Interviews
If you want daily verified updates on QA, QC, Pharmacovigilance, Clinical Research, and Pharma Walk-In Interviews, join Pharma Duniya’s official channels and never miss an opportunity.
✅ Join our WhatsApp Group ✅ Join our Telegram Channel
📌 Get verified pharma job alerts, interview tips, resume guidance, and student career support directly on your phone.
Freshers Pharma Jobs in India 2026 – Best Opportunities for Beginners (Freshers Pharma Jobs in India) Introduction The pharmaceutical industry in India is one of the fastest-growing sectors, offering a wide range of career opportunities for fresh graduates. With the expansion of pharmaceutical manufacturing, clinical research, regulatory affairs, and biotechnology, there is a rising demand for skilled professionals across multiple domains. Freshers who have completed B.Pharm, M.Pharm, B.Sc, M.Sc, or related life science courses often look for entry-level jobs to start their careers. In 2026, pharmaceutical companies, CROs, and healthcare organizations are actively hiring freshers for various roles in production, quality control, quality assurance, clinical research, and regulatory departments. This guide provides complete information about freshers' pharma jobs in India, including job roles, eligibility, salary, skills, and tips to get hired quickly. Why Choose a Career...
Global Pharma Hiring 30 Drug Safety Trainee in Bangalore 2026 | Pharmacovigilance Jobs for Freshers (Global Pharma Hiring 30 Drug Safety Trainees) INTRODUCTION Pharmacovigilance industry India me tezi se grow kar rahi hai aur 2026 me Drug Safety freshers ke liye bahut achhe career opportunities open ho rahe hain. Ek reputed Global Pharmaceutical Company ne Bangalore location ke liye 30 Drug Safety Trainee positions announce ki hain. Yeh role un candidates ke liye best hai jo Pharmacovigilance, Adverse Event Processing, aur Clinical Safety me apna career start karna chahte hain. Agar aap B.Pharm, M.Pharm, PharmD ya MSc Life Sciences background se ho aur Drug Safety me entry lena chahte ho to yeh opportunity aapke liye perfect starting point ho sakti hai. Company proper training, global exposure aur long-term career growth provide karegi. ABOUT THE COMPANY Hiring company ek globally recognised pharmaceutical organisation hai jo Drug Safety, Clinical Research, aur Pharmacovigilanc...
Mankind Pharma Walk-in Drive 2026 | QA, QC & Production Jobs in Udaipur & Behror (Mankind Pharma Walk-in Interview 2026) INTRODUCTION India ki top pharmaceutical companies me se ek Mankind Pharma ne 2026 ke liye ek badi Walk-in Interview Drive announce ki hai. Yeh hiring drive un candidates ke liye ek golden opportunity hai jo Quality Assurance (QA), Quality Control (QC), aur Production departments me apna career banana chahte hain. Agar aap pharma ya chemistry background se aate hain aur GMP environment, API ya formulation units me kaam kar chuke hain, to yeh walk-in interview aapke liye perfect ho sakta hai. Mankind Pharma apne Udaipur aur Behror (Rajasthan) manufacturing plants ke liye experienced professionals ko hire kar rahi hai, jiska interview Indore location par conduct hoga. ABOUT THE COMPANY – MANKIND PHARMA Mankind Pharma Limited India ki fastest growing pharmaceutical company me se ek hai. Company ki shuruaat 1995 me hui thi aur aaj yeh comp...
Biomapas Pharmacovigilance Jobs - 2026 | Remote PV Specialist (Case Processing) Hiring (Biomapas Pharmacovigilance Jobs - 2026) Introduction If you are looking to start or grow your career in pharmacovigilance and drug safety, this is an excellent opportunity. Biomapas (Delta PV division) is hiring Pharmacovigilance Specialists for remote roles. With the increasing demand for drug safety professionals worldwide, this role offers strong exposure to ICSR case processing, regulatory compliance, and global pharmacovigilance operations. Whether you are a fresher or have some PV experience, this opportunity can help you build a solid career in clinical research and drug safety. Looking for the best multivitamin? Here is the top recommendation: 👉 HealthKart Multivitamin – Best for Daily Energy 👉 Buy Now on Amazon (Best Price) About The Company Biomapas is a globally recognized Contract Research Organization (CRO) specializing in pharmacovigilance, regulatory affairs, and clinical r...
Parexel Hiring Patient Safety Associate I in Mohali 2026 | Pharmacovigilance Career Opportunity (Parexel Hiring Patient Safety Associate I in Mohali) Introduction If you are looking to start your career in pharmacovigilance and drug safety, this opportunity from Parexel is highly valuable. The company is hiring for the role of Patient Safety Associate I in Mohali, India, which is ideal for freshers and early-career professionals in pharmacy and life sciences. With the growing demand for drug safety professionals in 2026, roles like Patient Safety Associate are becoming one of the best entry points into the clinical research and pharmacovigilance industry. This job provides hands-on experience in ICSR processing, MedDRA coding, safety reporting, and global regulatory compliance. About The Company Parexel is a globally recognized Contract Research Organization (CRO) that provides clinical research, consulting, and regulatory services to pharmaceutical, biotechnology, and medical...
Lok-Beta Pharmaceuticals Hiring Freshers 2026 | QA, Production, RA & CQA Trainee Jobs (Lok-Beta Pharmaceuticals Hiring Freshers 2026) Introduction If you are a fresher looking to start your career in the pharmaceutical industry, this is a golden opportunity for you. Lok-Beta Pharmaceuticals is hiring fresh candidates for multiple trainee roles across Quality Assurance (QA), Production, Regulatory Affairs (RA), and Clinical Quality Assurance (CQA). This hiring drive is specially designed for candidates who want to gain practical exposure in GMP-regulated pharmaceutical manufacturing. Whether you are a B.Pharm, M.Pharm, or science graduate, this opportunity can help you build a strong foundation in pharma careers. About The Company Lok-Beta Pharmaceuticals is a well-established pharmaceutical manufacturing company in India, known for its commitment to quality, compliance, and innovation. The company operates advanced manufacturing facilities that follow global regulatory sta...
"Top 50 IPQA Interview Questions and Answers – Pharma Duniya" (Top 50 IPQA Interview Questions and Answers) Introduction In-Process Quality Assurance (IPQA) is one of the most important roles in pharmaceutical manufacturing. Whether you are a B.Pharm fresher , M.Pharm graduate , or an experienced QA professional , cracking an IPQA interview requires strong knowledge of GMP, documentation, deviations, BMR, audits, and compliance . In this article, Pharma Duniya brings you the Top 50 IPQA Interview Questions and Answers , specially designed for pharma company interviews . These questions are commonly asked in tablet, capsule, injectable, syrup, API, and OSD manufacturing plants . What is IPQA? (Quick Overview) IPQA (In-Process Quality Assurance) ensures that pharmaceutical manufacturing activities are carried out as per approved procedures, GMP guidelines, and regulatory requirements during production and packing. IPQA acts as a bridge between production and quality ....
Share on WhatsApp
