ProRelix Research Hiring – Multiple position in Clinical research | Pune

ProRelix Research, a fast‑growing organization in the clinical research and life sciences domain, is hiring for multiple positions at its Pune, India location. These opportunities are suitable for early to mid‑career professionals looking to grow their careers in clinical operations, data management, and quality functions.

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🏢 About Company

ProRelix Research is a clinical research organization focused on delivering quality‑driven clinical trial services across the life sciences industry. The company supports pharmaceutical, biotechnology, and healthcare clients through clinical operations, data management, and quality & training services.

ProRelix Research is known for its process‑oriented approach, strong focus on GCP compliance, and hands‑on involvement in end‑to‑end clinical research activities. The organization works closely with study teams and sites to ensure trials are conducted accurately, ethically, and on time.

📊 Job Role

• Position: 
  • Clinical Trial Assistant – I
  • Senior Clinical Data Associate
  • Senior Clinical Research Associate (CRA)
  • Quality and Training Executive
• Department: Clinical Research
• Location: Pune,India
• Experience: 0 to 6 years
• Qualification: B.Pharm, M.pharm
• Job Type: Full-Time
• Last Date of application: Not provided

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📌 Available Positions & eligibility

1. Clinical Trial Assistant I :
   • Openings: 01
   • Experience:0–2 years
   • Ideal for: Freshers or early‑career candidates starting in clinical trial operations
2. Senior Clinical Data Associate:
   • Openings: 01
   • Experience:5–6 years
   • Ideal for: Experienced CDM professionals with strong data review and quality control experience
3. Senior Clinical Research Associate (CRA):
   • Openings: 01
   • Experience:3–5 years
   • Ideal for: CRAs with hands‑on site monitoring and trial management experience
4. Quality and Training Executive
   • Openings: 01
   • Experience:2–5 years
   • Ideal for: Professionals with experience in GCP training, audits, and quality compliance
     

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🎓 Qualification Required

✅ General Eligibility (For All Roles)

• A Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field.
• Good understanding of clinical research basics and GCP principles (role‑specific depth may vary).
• Ability to work in a team‑based, process‑driven environment.
• Basic computer knowledge, especially MS Word, Excel, and Outlook.
• Good communication skills and attention to detai

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🧠 Skills Needed

• Basic understanding of clinical research and clinical trial processes.
• Familiarity with Good Clinical Practice (GCP) guidelines and why compliance is important.
• Strong attention to detail, especially while handling documents, data, or reports.
• Good organizational skills to manage tasks, timelines, and study‑related records.
• Ability to follow SOPs, instructions, and processes carefully.
• Comfortable using MS Word, Excel, and Outlook for daily work.

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⭐ Job Role Insight

• The Clinical Trial Assistant – I role is a strong starting point for freshers. It focuses on documentation, coordination, and study support, helping candidates understand how clinical trials work in real life.
• The Senior Clinical Data Associate role ensures that clinical trial data is correct, complete, and reliable. This role directly impacts data quality, which is critical for study analysis and regulatory submissions.
• The Senior Clinical Research Associate (CRA) role is key to site monitoring and trial execution. CRAs act as the link between study sites and sponsors, ensuring trials follow protocols and GCP guidelines.
• The Quality and Training Executive role supports compliance, audits, SOPs, and training programs. This role helps maintain high standards across all clinical activities.

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🎯 Who Should Apply

You should consider applying to ProRelix Research if you:

• Have a degree in Life Sciences, Pharmacy, Nursing, or a related healthcare field.
• Are a fresher or early‑career professional looking to enter clinical research
  (especially for Clinical Trial Assistant – I).
• Have relevant experience in clinical data management, site monitoring, or quality functions
  (for senior roles).
• Are interested in clinical trials, data accuracy, patient safety, and regulatory compliance.
• Like working with documents, data, and structured processes.

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💰 Salary Details

• The salary offered is competitive and role‑based, aligned with industry standards.Final compensation depends on:
  • Role and experience level
  • Skill set and interview performance
  • Responsibilities of the position

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💡 Preparation Tips

• Read the job role carefully (CTA, CDM, CRA, or Quality).
• Be clear about what support you’ll provide—documentation, data review, site coordination, monitoring, or quality activities.
• You don’t need to know everything, but you should understand how your role supports clinical trials.

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🔗 Application Process

Interested candidates should apply only through the official company career website using the link provided below.

Or you can send resume to below email

📧 Email your resume to:
career@prorelixresearch.com

📍 Job Location: Pune, India
📅 Experience Levels: Fresher to Experienced (role‑specific)

Please mention the position name you are applying for in the email subject line to help review your profile quickly.

Important Disclaimer:This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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