Sameer sapehia profile photo 1 on Tal

Sameer sapehia

Clinical Research & Patient Access Specialist | 6+ Yrs in Trials, PSPs, ICH-GCP | Driving Compliance & Patient Outcomes

India

6+ years of work experience

Neovance
May 20233 yrs 1 moPresent

Hybrid

Indira IVF Group
Nov 20227 mosMay 2023

On-site

Pushpawati Singhania Hospital Research Institute
Nov 20216 mosApr 2022

On-site

Institute Of Liver And Biliary Sciences
Jan 20201 yr 3 mosMar 2021

New Delhi, Delhi

Christian Medical College & Hospital
Oct 20181 yr 2 mosNov 2019

Ludhiana, Punjab, India

Education

ANOVUS INSTITUTE OF CLINICAL RESEARCH

Diploma in Clinical Research, Clinical research

ANOVUS INSTITUTE OF CLINICAL RESEARCH

20182018

Bachelor of Pharmacy - BPharm, Pharmacology, Pharmaceutical science, Pharmacognosy

Rayat Bahara Institute of Pharmacy

20124 yrs2016

Join Sameer and 10k+ other professionals on

Tal Boss

Tal is the app where bosses meet engineers & builders directly, without middlemen

Download Tal Boss

Sameer sapehia on Tal

Headline

Clinical Research & Patient Access Specialist | 6+ Yrs in Trials, PSPs, ICH-GCP | Driving Compliance & Patient Outcomes

About

I am a Clinical Research and Patient Access professional with over 6 years of experience supporting clinical trials, reimbursement programs, and patient support initiatives across national and international studies. With a Bachelor’s degree in Pharmacy and hands-on expertise in regulatory compliance, I bridge scientific knowledge with operational execution. In my current role as Program Specialist, I manage end-to-end patient support workflows, coordinate with healthcare providers, sponsors, and vendors, to ensure high-quality service delivery. I have helped maintain 100% compliance with ICH-GCP, HIPAA, and PHI requirements while improving turnaround times and reducing operational errors through workflow optimization. Previously, as a Clinical Research Coordinator across multiple hospital and academic sites, I supported site start-up, patient recruitment, informed consent, AE/SAE reporting, TMF documentation, and monitoring visit readiness. I am proficient in Veeva Vault, REDCap, CTMS, and TMF systems, ensuring accurate and audit-ready data at all times. What drives me is improving access to therapies while ensuring ethical, compliant, and efficient trial execution. I am now seeking opportunities in Clinical Trial Management, Patient Access Programs, and Global Clinical Operations where I can contribute to scalable, patient-centric research delivery. Keywords: Clinical Trials, Patient Access, Program Specialist, ICH-GCP, Medical science Liasion, CTMS, Regulatory Compliance, Safety Reporting, Reimbursement Coordination, Global Clinical Operations

Location

India

Work experience

Program Specialist at Neovance, May 2023 - Present · 3 yrs 1 mo, Hybrid

Clincal reserach Coordinator at Indira IVF Group, Nov 2022 - May 2023 · 7 mos, On-site

Clincal reserach Coordinator at Pushpawati Singhania Hospital Research Institute, Nov 2021 - Apr 2022 · 6 mos, On-site

Clinical research coordinator at Institute Of Liver And Biliary Sciences, Jan 2020 - Mar 2021 · 1 yr 3 mos, New Delhi, Delhi

Clinical Research Coordinator at Christian Medical College & Hospital, Oct 2018 - Nov 2019 · 1 yr 2 mos, Ludhiana, Punjab, India

Education

Diploma in Clinical Research, Clinical research, ANOVUS INSTITUTE OF CLINICAL RESEARCH

Bachelor of Pharmacy - BPharm, Pharmacology, Pharmaceutical science, Pharmacognosy, Rayat Bahara Institute of Pharmacy

Sameer sapehia - Program Specialist in India | Tal