"Script Assist Hiring Clinical Operations Specialist – Remote India | Pharmacovigilance & Healthcare SaaS Jobs 2026"

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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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"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"

"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"



(ProPharma Hiring Pharmacovigilance)



Are you passionate about drug safety and pharmacovigilance? ProPharma, a trusted global leader in regulatory sciences, clinical research, and drug safety, is inviting applications for the Pharmacovigilance Safety Scientist role in India. This position offers an excellent opportunity to work on global projects and contribute to improving patient safety worldwide.


Key Responsibilities:-

As a Pharmacovigilance Safety Scientist at ProPharma, you will be responsible for:

  • Authoring aggregate safety reports such as PSURs, PBRERs, PADERs, Annual Reports, ACO, and DSUR.
  • Developing and maintaining Risk Management Plans (RMPs).
  • Preparing Signal Management Reports and conducting literature searches.
  • Reconciling process trackers and validating extracted data.
  • Generating and reviewing line listings from safety databases.
  • Supporting ad-hoc pharmacovigilance activities as per project requirements.
  • Ensuring all deliverables meet ICH-GCP, FDA, EMA, and global PV regulations.
  • Contributing to SOPs, deviations, and CAPA activities.
  • Analyzing large volumes of safety data with precision and accuracy.


Required Qualifications & Skills:-

  • Education: Bachelor’s/Master’s in Pharmacy, Nursing, Life Sciences, or related health sciences.
  • Experience: Minimum 2+ years in pharmacovigilance, with expertise in medical writing, signal detection, or literature review.
  • Strong understanding of global PV regulations.
  • Excellent communication, writing, and analytical skills.
  • Proficiency in MS Office tools and PV database applications.
  • Ability to work in a matrix and multicultural environment.


Why Join ProPharma?

  • Be part of a global leader in pharmacovigilance and regulatory sciences.
  • Contribute to patient safety and global healthcare improvement.
  • Opportunity to work with a collaborative, diverse, and inclusive team.
  • Strong career growth in drug safety, PV, and medical writing.


How to Apply:-

Interested candidates can apply directly through the official link below:

๐Ÿ‘‰ Apply Here – Pharmacovigilance Safety Scientist at ProPharma India


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