2 jobs in Latinum HR Solutions
Clinical Safety Physician
Posted today
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Job Description
We're Hiring | Clinical Safety Physician (PSL) | Life Sciences
We are looking for a highly motivated Clinical Safety Physician to join a dynamic Life Sciences team. This opportunity is ideal for medical professionals with expertise in Pharmacovigilance, Clinical Safety, and Drug Safety who are passionate about ensuring patient safety and regulatory excellence.
Eligibility Criteria
• Qualification: MBBS/MD
• Location : PAN India
• Experience : 10+ Years
• Budget : Upto 25 LPA (Depending on Exp)
• Relevant experience in Clinical Safety, Pharmacovigilance, Drug Safety, or Clinical Research
Key Responsibilities
• Conduct medical review and scientific evaluation of safety data and literature.
• Perform signal detection, validation, assessment, and contribute to signal management activities.
• Author and review aggregate safety reports, including DSURs, PBRERs, Risk Management Plans (RMPs), and Drug Safety Reports (DSRs).
• Review Clinical Study Reports (CSRs), Individual Case Safety Reports (ICSRs), and provide expert medical input on safety-related matters.
• Ensure compliance with global regulatory guidelines and pharmacovigilance processes.
• Collaborate with cross-functional teams, support audits, and provide medical guidance to stakeholders.
• Contribute to process improvements, scientific discussions, and strategic safety initiatives.
Preferred Skills
• Strong knowledge of Pharmacovigilance, Clinical Safety, and Regulatory Affairs
• Experience in Signal Management and Aggregate Report Authoring
• Excellent scientific writing, analytical, and problem-solving skills
• Strong communication and stakeholder management abilities
If you meet the above criteria or know someone who would be a great fit, feel free to share your updated resume at &
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Manager Clinical Data Management
Posted 3 days ago
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Job Description
We are hiring Senior Manager – Clinical Data Management (VEEVA) for one of our leading BPO clients .
We are looking for professionals with strong experience in Clinical Data Management, vendor oversight, and managing global clinical studies.
Location : Pan India
Work Mode : Hybrid / Onsite
Experience : 8+ Year
Education : Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, or a related field
Key Responsibilities
- Lead Clinical Data Management activities for global clinical studies
- Manage CROs and third-party vendors to ensure quality and timely deliver
- Coordinate with cross-functional teams to meet project milestone
- Handle EDC setup, data review, query management, and database lock activities
- Prepare data validation plans, edit checks, reconciliation plans, and study documentation
- Ensure compliance with ICH-GCP, GxP, and CDISC standard.
- Support regulatory submissions and maintain Trial Master File (TMF)
- Monitor project timelines, budgets, and drive process improvement.
Required Ski
- Experience in Clinical Data Management
- Hands-on experience with Veeva is mandatory.
- Strong knowledge of EDC, CDISC, ICH-GCP, and GxP guidelines.
- Experience managing CROs and external vendors.
- Hands-on experience with data review, query management, and database lock.
- Excellent communication and stakeholder management skills.
Interested candidates can share their updated CV at: &
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