Current jobs related to Clinical Trial Lead, Immunology and Neuroscience, Medical Evidence Generation - Princeton - Bristol Myers Squibb


  • Princeton, New Jersey, United States Bristol-Myers Squibb Company Full time

    Position Overview:As a Lead Global Clinical Trial Coordinator, you will engage across diverse therapeutic domains and research phases, partnering with multidisciplinary global teams to manage the operational elements of international clinical research projects from protocol formulation to the completion of the clinical study report.Key Responsibilities:Serve...


  • Princeton, United States Endeavor Consulting Group Full time

    Job DescriptionJob DescriptionEndeavor Consulting Group, a leading consulting firm specializing in the pharmaceutical industry, is seeking a highly skilled and experienced Sr. Consultant, Clinical Trials. As a key member of our team, you will play a critical role in assisting our clients with the design, implementation, and improvement of clinical trials....


  • Princeton, United States Endeavor Consulting Group Full time

    Job DescriptionJob DescriptionEndeavor Consulting Group, a leading consulting firm specializing in the pharmaceutical industry, is seeking a highly skilled and experienced Sr. Consultant, Clinical Trials. As a key member of our team, you will play a critical role in assisting our clients with the design, implementation, and improvement of clinical trials....


  • Princeton, United States Genmab Full time

    At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in...


  • Princeton, New Jersey, United States Endeavor Consulting Group Full time

    Position OverviewEndeavor Consulting Group, a premier consulting firm in the pharmaceutical sector, is in search of a highly qualified and seasoned Senior Clinical Trials Consultant. In this pivotal role, you will significantly contribute to the enhancement and execution of clinical trials, thereby influencing the advancement of groundbreaking...


  • Princeton, New Jersey, United States Endeavor Consulting Group Full time

    Position OverviewEndeavor Consulting Group, a premier consulting firm in the pharmaceutical sector, is on the lookout for a highly qualified and seasoned Senior Clinical Trials Consultant. In this pivotal role, you will significantly contribute to the enhancement and execution of clinical trials, thereby influencing the advancement of groundbreaking...


  • Princeton, New Jersey, United States Endeavor Consulting Group Full time

    Position OverviewEndeavor Consulting Group, a premier consulting firm dedicated to the pharmaceutical sector, is in search of a highly qualified and seasoned Senior Clinical Trials Consultant. In this pivotal role, you will significantly contribute to our clients' efforts in the design, execution, and enhancement of clinical trials. This position offers a...


  • Princeton, United States Sun Pharmaceutical Industries, Inc. Full time

    Title: Director, Medical Affairs NA – Biologics Lead Sun Pharmaceuticals Industries Inc. is the fourth largest generic pharmaceutical company in the world, and rapidly building our brand presence. We manufacture, market and distribute pharmaceuticals to the nation’s largest wholesalers, distributors, warehousing and non-warehousing chain drugstores...


  • Princeton, New Jersey, United States Bristol Myers Squibb Company Full time

    Working with UsChallenging. 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...


  • Princeton, United States Bristol Myers Squibb Company Full time

    Working with UsChallenging. 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...


  • Princeton, United States Sun Pharmaceutical Industries, Inc. Full time

    Title: Director, Medical Affairs NA – Biologics Lead  Sun Pharmaceuticals Industries Inc. is the fourth largest generic pharmaceutical company in the world, and rapidly building our brand presence. We manufacture, market and distribute pharmaceuticals to the nation’s largest wholesalers, distributors, warehousing and non-warehousing chain drugstores as...


  • Princeton, New Jersey, United States Clinical Resource Network (CRN) Full time

    Position Overview:We are seeking a qualified individual to assume the role of Medical Affairs Consultant. This position is entirely remote.Key Responsibilities:Engaging with Medical Affairs colleagues and external partners to implement asset strategies and tactical plans while effectively utilizing resources and adhering to established timelines.Monitoring...


  • Princeton, United States SYSTEM EDGE (USA) L.L.C. Full time

    Job Title: Clinical Trial Transparency ConsultantWork Location: Remote, Princeton, NJEssential Duties and Responsibilities: Perform required clinical trial registration and/or results disclosure activities as necessary.Assess the process between Clinical Management and the CTT&D team, suggesting improvements where needed.Collaborate with the system...


  • Princeton, United States SYSTEM EDGE (USA) L.L.C. Full time

    Job Title: Clinical Trial Transparency ConsultantWork Location: Remote, Princeton, NJEssential Duties and Responsibilities: Perform required clinical trial registration and/or results disclosure activities as necessary.Assess the process between Clinical Management and the CTT&D team, suggesting improvements where needed.Collaborate with the system...


  • Princeton, United States Bristol Myers Squibb Company Full time

    Working with UsChallenging. 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...


  • Princeton, New Jersey, United States Clinical Resource Network (CRN) Full time

    Position Overview:We are seeking a qualified individual to assume the role of Medical Affairs Consultant. This position offers the flexibility of remote work.Key Responsibilities:Engaging with Medical Affairs teams and external partners to implement asset strategies and tactical initiatives while optimizing resource allocation and adhering to established...


  • Princeton, New Jersey, United States Bristol Myers Squibb Company Full time

    Working with UsChallenging. 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...


  • Princeton, United States Bristol Myers Squibb Company Full time

    Working with UsChallenging. 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...


  • Princeton, New Jersey, United States SYSTEM EDGE (USA) L.L.C. Full time

    Position Title: Clinical Trial Transparency ManagerLocation: RemoteKey Responsibilities:Guide the Transparency team on the complete Clinical Trial process and execution of trials.Conduct necessary clinical trial registration and results disclosure activities.Evaluate the workflow between Clinical Management and the Clinical Trial Transparency & Disclosure...


  • Princeton, United States Clinical Resource Network (CRN) Full time

    Our client is looking to fill the role of Medical Affairs Consultant. This position will be fully remote.Responsibilities:Collaborating with Medical Affairs colleagues and external vendors to execute asset strategy and tactical plans with appropriate use of resources and according to developed timelinesTracking priority Medical Affairs tactics and...

Clinical Trial Lead, Immunology and Neuroscience, Medical Evidence Generation

3 months ago


Princeton, United States 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 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.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

The Clinical Trial Lead, I&N will be responsible for the day-to-day oversight of the MEG BoW which provides scientific expertise necessary to design and deliver Medical Affairs Sponsored Trials, execute on the ISR book of work, and co-develop Integrated Evidence Plan

The Clinical Trial Lead for assigned asset is responsible for driving the development, tracking, and maintenance of the Integrated Evidence Plan, provide oversight of Investigator Sponsored Research (ISR) Book of Work

Key Responsibilities
Clinical Scientist on assigned MASTs, ensuring quality execution of deliverables for all phases of assigned MASTs (start-up/conduct/closure), through activities such as:Protocol design concept sheet, Protocol and ICF developmentSite-facing activitiesCRA training materialsData quality activities; ensure consistent, quality data review across trial teamsInvestigator Meetings, SIVs, Advisory Board, and Study committee (e.g., DMC) activitiesClinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, regulatory responses)Develop IEP that reflects asset strategy, market priorities, and medical data generation support in partnership with cross functional teams including (but not limited to) GDD, Translational Development, & HEORDevelop Areas of Interest based on key open data questions identified in the IEP with market input in collaboration with WWMIdentify ISR studies at risk for failing to meet timelines and negotiate mitigation plans with key internal stakeholders and investigatorsAssist in reviews of concepts through RFP process, including providing context for ongoing book of work, area of interest development, and upcoming data read outsMEG representative at AIMs for assigned asset and AIMs working team leadQualifications & ExperienceDegree in Life Sciences (MD, PhD, Pharm D, MS, RN, or other scientific field preferred) with at least 2 years' experience with clinical trial oversightDemonstrated proficiency in driving and managing company-sponsored clinical trials and leading teams (e.g., Clinical Scientist team lead)Demonstrated track record of leadership in a complex, matrix environment. Experience delivering successful results in a variety of business situations.Excellent communication skills and experience with difficult discussions.Successful track record of leading through influence and working across complex, global organizational matricesAble to analyze, interpret, and present dataAbility to self-supervise, and act independently to identify/resolve program level issuesProficient critical thinking, problem-solving, decision-making skills, oral and written communication skillsStrong leadership presenceCommitment to QualityAdaptable / FlexibleExhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externallyPromotes a culture of scientific excellence, multidisciplinary problem solving, teamwork, consistency, flexibility, execution, quality, and effective communication#LI-Hybrid

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

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 adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility 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.