Clinical Trial Registration Senior Specialist – Global Clinical Operations
Location: Hyderabad, Telangana, India
Employment Type: Full-Time, On-Site
Category: Clinical Operations / Trial Registration / Regulatory Compliance
Experience Required: Minimum 3 Years
Company: Bristol Myers Squibb (BMS)
Role Overview
Bristol Myers Squibb (BMS) is seeking a Clinical Trial Registration Senior Specialist to join our Global Development Operations team in Hyderabad. This role plays a key part in ensuring that clinical trials are accurately registered and maintained in public registries, including ClinicalTrials.gov, EU PAS, and other country-specific registries.
The Clinical Trial Registration Specialist will collaborate with cross-functional teams, including trial managers, clinical scientists, statisticians, and regulatory experts, to ensure timely, high-quality, and compliant registration of clinical trial protocols. This is an excellent opportunity for professionals with a background in clinical research, regulatory compliance, or clinical trial transparency to advance their careers in a global pharmaceutical environment.
Key Responsibilities
Drive protocol registration processes, ensuring timely and accurate posting of clinical trial information in public registries (ClinicalTrials.gov, EU PAS, and other applicable registries)
Collaborate with cross-functional teams including Global Trial Managers, Operations Leads, Clinical Trial Physicians, Statisticians, and Regulatory stakeholders to ensure data consistency and protocol alignment
Provide maintenance support for assigned trial records to ensure information is accurate and up-to-date
Submit registration updates and amendments within global regulatory timelines
Maintain study trackers and ensure weekly updates on trial registration status
Educate stakeholders on registry requirements, NIH review criteria, and proper completion of registration forms
Support registration of clinical trials beyond US/EU markets as needed
Ensure adherence to internal SOPs, NIH guidelines, and global regulatory compliance standards
Required Qualifications and Experience
Bachelor’s degree in Life Sciences, Pharmacy, or a Science-related field
Minimum 3 years of work experience, preferably in a biopharmaceutical company or CRO
Experience in clinical research, quality, regulatory, compliance, or clinical trial execution preferred
Familiarity with clinical trial transparency and registry submissions
Key Competencies
Proficient in Microsoft Excel and other analytical tools
Strong organizational, multitasking, and time management skills
Excellent written and verbal communication skills in English
Ability to work independently and collaboratively in a multi-functional, global team
Attention to detail and commitment to high-quality work
Ability to adapt to multiple therapeutic areas and clinical study types
About Bristol Myers Squibb
At BMS, we are dedicated to transforming patients’ lives through science™. Our employees work on meaningful, life-changing projects every day—from breakthrough therapies in oncology and cell therapy to global clinical trial programs. With a culture emphasizing passion, innovation, urgency, accountability, inclusion, and integrity, BMS empowers employees to grow their careers while making a global impact.
On-Site Protocol: This is a site-essential role, requiring full-time presence at the Hyderabad facility to foster collaboration, productivity, and innovation.
Supporting People with Disabilities: BMS is committed to providing reasonable accommodations and a transparent recruitment process for individuals with disabilities.
Data Privacy and Fraud Protection: BMS does not request payments, social security numbers, or financial information during recruitment. All candidate data is handled per global privacy standards.
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