Acme Generics Regulatory Affairs Executive Recruitment 2026 | B.Pharm M.Pharm Jobs in Ahmedabad for EU Regulatory Affairs Professionals

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Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026 (Acme Generics Regulatory Affairs Executive Recruitment 2026) Introduction Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions. Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards. About Acme Generics Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketin...

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"Kickstart Your Career as a Clinical Research Coordinator in Dehradun – KV Clinical Research is Hiring!"

"Clinical Research Coordinator Job in Dehradun – Join KV Clinical Research Pvt Ltd"


Are you a qualified pharma or life sciences graduate looking to grow your career in clinical research? KV Clinical Research Pvt Ltd, a reputed Site Management Organization (SMO), is inviting applications for the post of Clinical Research Coordinator (CRC) at its Dehradun site. This is an excellent opportunity to contribute to regulated clinical trials and gain hands-on industry experience in a supportive, dynamic environment.


Position: Clinical Research Coordinator (CRC) – Dehradun:-

📍 Location:

Dehradun, Uttarakhand, India

🏢 Company:

KV Clinical Research Pvt Ltd


🔹 Key Responsibilities:-

As a Clinical Research Coordinator, you will be responsible for ensuring the seamless operation of clinical trial activities at the site. Key duties include:

  • Coordinating daily trial operations as per protocol and regulatory standards
  • Managing patient recruitment, screening, informed consent, and follow-ups
  • Maintaining proper documentation and ensuring accurate data collection
  • Communicating with investigators, sponsors, and ethics committees
  • Ensuring compliance with ICH-GCP and SOPs
  • Maintaining patient interaction and documentation in Hindi, English, and local languages
  • Reporting progress and updates to the project team

Required Qualifications and Skills:-

Eligibility Criteria:

  • Educational Background: B.Pharm, M.Pharm, B.Sc, or M.Sc in a relevant field
  • Language Skills: Proficiency in Hindi, English, and regional languages (e.g., Garhwali, Kumaoni)
  • Knowledge: Familiarity with GCP, clinical research guidelines, and trial documentation
  • Experience: Prior experience as CRC or in a clinical research setting preferred (Freshers may also apply)
  • Soft Skills: Strong interpersonal skills, team collaboration, and attention to detail

Why Join KV Clinical Research?

Choosing KV Clinical Research Pvt Ltd opens the door to a rewarding career in clinical research:

  • Real-Time Exposure: Work on cutting-edge clinical trials
  • Career Advancement: Build a solid foundation for a long-term pharma career
  • Learning Support: Access continuous training and mentoring
  • Work-Life Balance: Enjoy working in the peaceful and scenic city of Dehradun
  • Collaborative Environment: Be part of a friendly and forward-thinking research team

How to Apply:-

If you meet the qualifications and are ready to make a difference in the field of clinical research, follow the steps below:

  1. Update your CV – Emphasize your education, research skills, and language fluency
  2. Send your CV to: hr@kvclinicalresearch.com
  3. Subject Line: CRC Application – Dehradun

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