Current jobs related to Senior Specialist Clinical Trial Registration - hyderabad - Bristol Myers Squibb
-
Clinical Trial Registration Specialist
2 weeks ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeJob Summary We are seeking a highly skilled Clinical Trial Registration Specialist to join our team at Bristol Myers Squibb. As a key member of our clinical trials operations team, you will be responsible for preparing and providing operational support for the registration and maintenance of clinical trials into public registries in the US and EU. Key...
-
Clinical Trial Registration Specialist
6 days ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeAbout the RoleThe Clinical Trial Registration Sr. Specialist will report to the Clinical Trial Registration Lead, responsible for preparing and providing operational support for the registration and maintenance of clinical trials into public registries in US and EU.Key ResponsibilitiesThe successful candidate will drive the processes for assigned protocol...
-
Senior Clinical Trial Registration Specialist
2 weeks ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Clinical Trial Registration Specialist to join our team.Job SummaryThe Clinical Trial Registration Specialist will be responsible for preparing and providing...
-
Senior Clinical Trial Registration Specialist
3 weeks ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Clinical Trial Registration Specialist to join our team.Job SummaryThe Clinical Trial Registration Specialist will be responsible for preparing and providing...
-
Hyderabad, Telangana, India Bristol Myers Squibb Full timeTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking a highly skilled and experienced Senior Specialist Clinical Trial Registration to join our team.Job SummaryThe Senior Specialist Clinical Trial Registration will be responsible...
-
Clinical Trial Registration Specialist
6 days ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeAbout This RoleThe Clinical Trial Registration Sr. Specialist will report to the Clinical Trial Registration Lead, providing operational support for the registration and maintenance of clinical trials into public registries in the US and EU.Key ResponsibilitiesDrive the processes for assigned protocol registration activities, ensuring timely and high-quality...
-
Senior Clinical Trial Registration Specialist
4 weeks ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Clinical Trial Registration Specialist to join our team.Job SummaryThe Clinical Trial Registration Specialist will be responsible for preparing and providing...
-
Senior Specialist Clinical Trial Registration
5 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...
-
Clinical Trials Disclosure Specialist
4 weeks ago
Hyderabad, Telangana, India Lifelancer Full timeAbout the RoleLifelancer is seeking a highly skilled Clinical Trials Disclosure Specialist to join our team. As a key member of our team, you will be responsible for coordinating and developing multiple disclosures deliverables, ensuring compliance with industry guidelines and client requirements.Key ResponsibilitiesCoordinate registration, maintenance, and...
-
Clinical Trials Disclosure Specialist
3 weeks ago
Hyderabad, Telangana, India Lifelancer Full timeAbout the RoleLifelancer is seeking a highly skilled Clinical Trials Disclosure Specialist to join our team. As a key member of our team, you will be responsible for coordinating and developing multiple disclosures deliverables, ensuring compliance with industry guidelines and client requirements.Key ResponsibilitiesCoordinate registration, maintenance, and...
-
Clinical Trial Disclosure Specialist
6 days ago
Hyderabad, Telangana, India Lifelancer Full timeAbout the RoleWe are seeking a skilled Clinical Trial Disclosure Specialist to join our team at Lifelancer. The successful candidate will be responsible for coordinating and developing multiple disclosures deliverables, ensuring compliance with industry guidelines and client requirements.Key ResponsibilitiesCoordinate registration, maintenance, and results...
-
Hyderabad, Telangana, India Lifelancer Full timeAbout UsLifelancer is a talent hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.We are seeking a highly skilled Clinical Trial Transparency and Disclosure Specialist to join our team. As a Clinical Trial Transparency and Disclosure Specialist,...
-
Clinical Trial Disclosure Specialist
2 weeks ago
Hyderabad, Telangana, India Lifelancer Full timeJob SummaryThe Clinical Trial Disclosure Specialist will be responsible for coordinating and developing multiple disclosures deliverables, including compliant registry authoring and maintenance of information on public registries, document redaction, and/or plain language authoring, ensuring adherence to relevant industry guidelines and client styles and...
-
Clinical Trial Disclosure Specialist
1 week ago
Hyderabad, Telangana, India Lifelancer Full timeWe are seeking a skilled Clinical Trial Disclosure Specialist to join our team at Lifelancer. In this role, you will be responsible for the overall coordination and development of multiple disclosures deliverables, including compliant registry authoring and maintenance of information on public registries, document redaction, and/or plain language...
-
Hyderabad, India Lifelancer Full timeAbout the jobFor 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, Telangana, India Lifelancer Full timeAbout LifelancerLifelancer is a talent hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.The Clinical Trials Disclosure Specialist position is responsible for the overall coordination and development of multiple disclosures deliverables,...
-
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) 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) ProPharma...
-
Senior Manager for Clinical Trial Management
6 days ago
Hyderabad, Telangana, India Bristol Myers Squibb Full timeTransforming Lives through Clinical TrialsBristol Myers Squibb is at the forefront of innovative healthcare solutions, and we're seeking a Senior Manager, Global Submission Management, Clinical Trials to join our team.Key ResponsibilitiesManage a team of direct reports to ensure timely, compliant, and accurate delivery of core submission documents and...
Senior Specialist Clinical Trial Registration
2 months ago
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 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 fieldExperience 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 preferredKey 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.
