Shaishav Modh
Clinical Research Professional with expertise in Clinical Operations, Project and Vendor Management.
- Role
- Trial Vendor Senior Manager at Novartis
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Shaishav Modh
As a clinical research professional with over a decade of experience, I specialize in study delivery management, clinical operations, Vendor management and project oversight. I lead end-to-end study delivery, ensuring seamless execution through cross-functional collaboration and meticulous oversight of timelines, budgets, trial vendors, and quality metrics. Adept at leveraging project management tools, I empower teams to maintain compliance and operational excellence. My expertise includes managing vendors, optimizing trial master files, and supporting data-driven decision-making processes. I am motivated by a commitment to advancing clinical research through strategic planning and innovative problem-solving. Working with global stakeholders, I aim to drive impactful results that contribute to organizational goals and improve patient outcomes.
Experience
Trial Vendor Senior Manager
Sep 2025 — Present · Hyderabad, IN
Accountable for vendor-related operational trial deliverables across global clinical trials, ensuring timelines, budget, compliance, and quality standards. Collaborate as a core member of Clinical Trial Teams to oversee vendor selection, contracting, performance monitoring, and risk management. Lead vendor interfaces across central labs, eCOA/ePRO, IRT, imaging, diagnostics, and patient recruitment services. Drive study start-up excellence, optimize vendor strategy, and ensure high-quality service delivery throughout the trial lifecycle.
Education
Rajiv Gandhi University of Health Sciences
Bachelor of Pharmacy (BPharm), Pharmaceutical Sciences
2006 — 2010
Shree Vividh Laxmi Vidyamandir
Biology/Biological Sciences, General
Rajiv Gandhi University of Health Sciences
Doctor of Pharmacy (Pharm.D.), Pharmacotherapeutics, Clinical Research
2011 — 2014
Skills
- Ich-Gcp
- Healthcare
- Gcp
- U.s. Food and Drug Administration (Fda)
- Clinical Monitoring
- Clinical Trial Management System (Ctms)
- Clinical Trials
- Clinical Research
- Pharmacovigilance
- Clinical Administration
- Oncology
- Electronic Data Capture (Edc)
- Pharmaceutical Industry
- Life Sciences
- Biotechnology
- Regulatory Affairs
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