Script Assist Hiring Clinical / Medical Operations Specialist – Remote India (Healthcare SaaS Role) (Script Assist Hiring Clinical Operations Specialist) Healthcare technology companies are rapidly expanding their global operations, creating new opportunities for clinically qualified professionals who want to transition into non-patient-facing roles. If you are looking for remote pharmacovigilance jobs, clinical operations roles, or healthcare SaaS careers, this opportunity could be ideal. Script Assist is hiring a Clinical / Medical Operations Specialist – Platform Support for its remote India team. This is a full-time role aligned with UK business hours and focuses on regulated healthcare workflows, platform operations, audit compliance, and structured documentation. This position is particularly suitable for professionals with backgrounds in pharmacovigilance, medical information, clinical research, and healthcare compliance who want to move into tech-enabled clinical operations. ...
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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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