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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“KV Clinical Research Hiring Clinical Research Coordinator (CRC) in Deogarh, Jharkhand – Apply Now”

"KV Clinical Research Hiring Clinical Research Coordinator (CRC) in Deogarh, Jharkhand"



(KV Clinical Research Hiring)



KV Clinical Research Pvt Ltd, an emerging organization in the field of clinical trials and research management, is inviting applications for the position of Clinical Research Coordinator (CRC) in Deogarh, Jharkhand. This opportunity is ideal for pharmacy and life science graduates who are passionate about clinical research and looking to build a rewarding career in the pharmaceutical and healthcare industry.


Key Responsibilities:-

As a Clinical Research Coordinator (CRC) at KV Clinical Research, your primary responsibilities will include:

  • Assisting in planning, organizing, and coordinating clinical trials.
  • Ensuring compliance with regulatory guidelines and Good Clinical Practice (GCP).
  • Collecting, recording, and maintaining accurate patient data.
  • Supporting principal investigators in study-related activities.
  • Effective communication with sponsors, ethics committees, and site staff.
  • Preparing essential study documents and assisting during monitoring visits.


Required Qualifications:-

To apply for this role, candidates must meet the following criteria:

  • Education: B.Pharm, M.Pharm, B.Sc, or M.Sc in Life Sciences/Pharmacy.
  • Languages: Proficiency in Hindi, English, and the local regional language.
  • Experience: Both freshers and experienced professionals are welcome to apply.


Benefits of Joining KV Clinical Research:-

Working at KV Clinical Research Pvt Ltd offers several professional advantages, including:

  • Hands-on exposure to clinical trials and regulatory compliance.
  • Career growth opportunities in clinical research and allied healthcare fields.
  • Experience working with multi-disciplinary healthcare teams.
  • Opportunity to contribute to advancing medical science and patient care.


Job Location:-

  • City: Deogarh
  • State: Jharkhand
  • Organization: KV Clinical Research Pvt Ltd


How to Apply:-

Interested and eligible candidates can share their updated CV at:

📧 hr@kvclinicalresearch.com

 Don’t miss this opportunity to begin or grow your career in clinical research with KV Clinical Research Pvt Ltd. Apply today and take your first step toward becoming a part of India’s growing clinical trial ecosystem.


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