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MindPec Solutions is hiring Clinical Research Associates (CRAs) in Bengaluru and Delhi. This is a fantastic opportunity for professionals with 1 – 5 Years of experience in clinical research and regulatory documentation. If you’re eager to grow in clinical trial operations, AI-assisted documentation, and regulatory compliance, this role is tailor-made for you.
🔑 Key Responsibilities
- Author, review, and analyze essential clinical trial documents (Protocol, ICF, CSR, Safety/Efficacy Summaries, etc.)
- Develop, validate, and refine AI-driven document generation prompts
- Apply expertise in clinical trial phases, study design, and drug development
- Ensure compliance with ICH-GCP, FDA, and EMA guidelines
- Collaborate with cross-functional teams to ensure accuracy, compliance, and timely delivery
- Provide updates to project managers and flag potential risks proactively
🎓 Qualifications
- Bachelor’s/Master’s degree in Pharma, Life Sciences, Biotechnology, or related field
- 1 – 5 years of relevant clinical research/documentation experience
- Familiarity with regulatory standards (FDA, EMA, ICH-GCP)
- Strong analytical, documentation, and communication skills
- Experience with AI-assisted tools will be an added advantage
💼 Benefits of Joining MindPec Solutions
- Work with global clinical documentation projects
- Gain hands-on AI integration exposure in clinical research
- Opportunity to collaborate with leading multinational clients
- Competitive salary package (₹4,00,000 – ₹7,00,000 per annum)
- Professional growth in a fast-evolving healthcare R&D domain
📌 Application Process
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