Senior Specialist Clinical Trial Registration
1 week ago
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Position Summary / Objective
The Clinical Trial Registration Sr. Specialist will report to the Clinical Trial Registration Lead, prepare and provide operational support for the registration and maintenance of clinical trials into public registries in US and EU.
Position Responsibilities
Drives the processes for assigned protocol registration activities, resulting in timely, high-quality information posted on clinical trial registries (Clinicaltrials.gov and EU PAS).
Liaises with clinical team reviewers (Global Trial Managers, Operations Leads, Statisticians, Clinical Trial Physicians, Clinical Scientists, Development Leads, Patent Attorneys) and other stakeholders on all assigned trials to ensure trial registrations are accurate, consistent with the protocol and other source data, and reported in adherence to NIH guidelines.
Provides maintenance support to CT Registration Lead for assigned records, to ensure the consistent accuracy of information disclosed on Clinicaltrials.gov.
Submits registration updates to Clinicaltrials.gov on behalf of clinical team, within global regulatory timelines.
Maintains study trackers and ensures they are up to date every week.
Educates stakeholders, as needed, on NIH detailed review criteria for registrations as well as on the purpose and format of the different fields in the protocol registration form.
Degree Requirements
Bachelor’s degree, preferably in a Science-related field
Experience Requirements
Minimum of 3 years overall work experience, preferably in a biopharmaceutical or CRO company
Work experience in quality, regulatory, compliance, clinical research or drug development highly desirable
Work experience in clinical trial transparency or clinical trial execution work, or work experience related to quality and compliance in clinical research preferred
Key Competency Requirements
Demonstrated Excel and analytical skills
Ability to work in a multi-functional team and across multiple therapeutic areas
Demonstrated ability to work independently and seek out support when needed
Written and oral communication skills
Strong organizational skills with the ability to multitask and prioritize
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
-
hyderabad, India Bristol Myers Squibb Full timeWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Senior Specialist Clinical Trial Registration
3 months ago
Hyderabad, India Bristol Myers Squibb Full timeWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Hyderabad, India Lifelancer Full timeAbout the job For the past 20 years ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech med device and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the worlds largest RCO (Research Consulting Organization) ProPharma...
-
hyderabad, India Lifelancer Full timeAbout the job For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the worlds largest RCO (Research Consulting Organization),...
-
Associate Clinical Trial Leader
2 days ago
hyderabad, India Novartis Full timeYour responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...
-
Associate Clinical Trial Leader
4 months ago
hyderabad, India Novartis Full timeYour responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...
-
Hyderabad, India Bristol Myers Squibb Full timeWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
hyderabad, India Lifelancer Full timeAbout thejob For the past 20 yearsProPharma has improved the health and wellness of patients byproviding advice and expertise that empowers biotech med device andpharmaceutical organizations of all sizes to confidently advancescientific breakthroughs and introduce new therapies. As the worldslargest RCO (Research Consulting Organization) ProPharma...
-
Hyderabad, India Lifelancer Full timeAbout thejob For the past 20 yearsProPharma has improved the health and wellness of patients byproviding advice and expertise that empowers biotech med device andpharmaceutical organizations of all sizes to confidently advancescientific breakthroughs and introduce new therapies. As the worldslargest RCO (Research Consulting Organization) ProPharma...
-
hyderabad, India Lifelancer Full timeAbout thejob For the past 20 yearsProPharma has improved the health and wellness of patients byproviding advice and expertise that empowers biotech med device andpharmaceutical organizations of all sizes to confidently advancescientific breakthroughs and introduce new therapies. As the worldslargest RCO (Research Consulting Organization) ProPharma...
-
Clinical Application Specialist
2 weeks ago
Hyderabad, India FutureMed Innovations Full timeJob descriptionThe Clinical Application Specialist will independently manage surgical cases and train surgical teams on the safe and effective use of our medical devices. This role requires collaboration with surgical teams, providing clinical support, and assisting with training programs for physicians and sales teams within the assigned territory.Location:...
-
Clinical Application Specialist
2 weeks ago
hyderabad, India FutureMed Innovations Full timeThe Clinical Application Specialist will independently manage surgical cases and train surgical teams on the safe and effective use of our medical devices. This role requires collaboration with surgical teams, providing clinical support, and assisting with training programs for physicians and sales teams within the assigned territory.Location: Delhi NCR and...
-
Senior Clinical Support Specialist
2 weeks ago
hyderabad, India GastroLab India Pvt. Ltd Full timeJob Title: Senior Clinical Support Specialist (SCSS)Location: Hyderabad, Kolkata, & New DelhiAbout GastroLab IndiaGastroLab India is a pioneering company in gastroenterology diagnostics, specialising in novel diagnostic tools like Electrogastrography (EGG) and other GI physiology test assays. We are committed to improving patient outcomes by helping...
-
Senior Clinical Support Specialist
2 weeks ago
Hyderabad, India GastroLab India Pvt. Ltd Full timeJob Title: Senior Clinical Support Specialist (SCSS) Location: Hyderabad, Kolkata, & New DelhiAbout GastroLab India GastroLab India is a pioneering company in gastroenterology diagnostics, specialising in novel diagnostic tools like Electrogastrography (EGG) and other GI physiology test assays. We are committed to improving patient outcomes by helping...
-
Associate Director – Bio-Clinical Studies
2 days ago
hyderabad, India Ferring Pharmaceuticals Full timeJob Description:Role: Associate Director – Bio-clinical studiesReporting to: Senior Director - Pharmaceutical DevelopmentLocation: HyderabadExperience: At least 15 years of industrial experience in the following:Drug product development in early to late phase clinical development.Hands on experience in BA-BE studies in healthy volunteers.Hands on...
-
Associate Director – Bio-Clinical Studies
3 months ago
Hyderabad, India Ferring Pharmaceuticals Full timeJob Description:Role: Associate Director – Bio-clinical studiesReporting to: Senior Director - Pharmaceutical DevelopmentLocation: HyderabadExperience: At least 15 years of industrial experience in the following:Drug product development in early to late phase clinical development.Hands on experience in BA-BE studies in healthy volunteers.Hands on...
-
Document Coordinator, Global Trial Acceleration
5 months ago
Hyderabad, Telangana, India Bristol-Myers Squibb Full time**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Document Coordinator, Global Trial Acceleration
5 months ago
Hyderabad, Telangana, India Bristol-Myers Squibb Full time**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Clinical Application Specialist
2 weeks ago
Hyderabad, India FutureMed Innovations Full timeJob description The Clinical Application Specialist will independently manage surgical cases and train surgical teams on the safe and effective use of our medical devices. This role requires collaboration with surgical teams, providing clinical support, and assisting with training programs for physicians and sales teams within the assigned territory. ...
-
Clinical Application Specialist
2 weeks ago
Hyderabad, India FutureMed Innovations Full timeJob descriptionThe Clinical Application Specialist will independently manage surgical cases and train surgical teams on the safe and effective use of our medical devices. This role requires collaboration with surgical teams, providing clinical support, and assisting with training programs for physicians and sales teams within the assigned territory.Location:...
