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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"SMOConnect Hiring Clinical Research Coordinator (CRC) Trainee in Uduppi, Karnataka | Clinical Research Jobs 2025"
(SMOConnect Hiring Clinical Research Coordinator (CRC) Jobs 2025)
If you’re a Life Science or Pharmacy graduate looking to start a career in clinical research, here’s an excellent opportunity. SMOConnect Clinical Research Services Pvt. Ltd is hiring Clinical Research Coordinator (CRC) Trainees for its site in Uduppi, Karnataka.
This is a full-time, on-site role ideal for fresh graduates who want hands-on exposure to clinical trial operations, regulatory documentation, patient recruitment, and site management under ICH-GCP guidelines.
This job is suitable for candidates searching for:
Clinical Research Coordinator jobs
CRC Trainee openings
Clinical research jobs for freshers
Clinical research jobs in Karnataka
Life Science & Pharmacy fresher jobs
Key Responsibilities:-
As a CRC Trainee, you will assist the clinical research team in daily site operations, including:
• Maintain source documents, CRFs, eCRFs, and Investigator Site File as per ICH-GCP
• Assist in site qualification, initiation, monitoring, and close-out visits
• Manage Investigational Product (IP) storage and temperature monitoring
• Coordinate Ethics Committee (EC) submissions and meetings
• Handle safety reporting within regulatory timelines
• Support patient screening, selection, and recruitment
• Assist with Informed Consent Process (ICF)
• Coordinate with local and central laboratories
• Ensure documentation accuracy and regulatory compliance
Eligibility & Qualifications:-
Educational Qualification
• B.Sc / M.Sc (Life Sciences)
• B.Pharm / M.Pharm
Experience
• Freshers are eligible
Skills Required
• Strong communication and documentation skills
• Basic understanding of clinical trials
• Knowledge of Kannada is mandatory (local patient interaction)
• Ability to work Monday–Saturday (day shift)
✔ Start your clinical research career with real-site exposure
✔ Learn ICH-GCP, site management, and regulatory workflows
✔ Work with experienced investigators and operations teams
✔ Fast-growth environment for fresh graduates
Clear comparison of roles, salary trends, growth prospects, and skillsets — perfect if you’re choosing a pharma career path.
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