Clinical trials Jobs in New Jersey

1 - 20 of 243 Jobs

Clinical - Clinical Trials Disclosure SpecialistJob Title - Clinical - Clinical Trials Disclosure Specialist

Net2Source Inc.Company Name - Net2Source Inc.

•

Madison, New Jersey, USA

Contract

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap Right Talent Right Time Right Place Right Price and acting as a Career Coach to our consultants. Job Description: Role is 50% onsite CW can work fr

R Developer/Statistical Analyst(FSP Remote in U.S./Canada only)Job Title - R Developer/Statistical Analyst(FSP Remote in U.S./Canada only)

TechData Service Company LLCCompany Name - TechData Service Company LLC

•

Remote or Bernards, New Jersey, USA

Full-time

Job DescriptionJob DescriptionR Developers In this role, you will design, develop, test, and maintain R programs which support the development of state-of-the-art reports and, at times, shiny applications, used by biostatisticians and statistical programmers worldwide. Within the Analytics and Reporting Tools (ART) team, you will contribute to multiple projects aimed at improving the success, efficiency, and quality of our trials from design to statistical reporting, data exploration, and visual

Senior Director, Real World Evidence - Hematology-Oncology, Data Science & Digital HealthJob Title - Senior Director, Real World Evidence - Hematology-Oncology, Data Science & Digital Health

Johnson & JohnsonCompany Name - Johnson & Johnson

•

Hopewell Township, New Jersey, USA

Full-time

Description This role will direct and lead efforts to bring innovative approaches to the use of Real World Evidence (RWE) to the Oncology Clinical Development Teams. You will have global leadership responsibilities for a wide range of activities, including capability and talent development, resource management and deployment, and supporting an organizational culture that promotes data-driven decision-making across all functions of Johnson & Johnson Innovative Medicine - R&D Oncology. You will b

Director, Clinical Research, ImmunologyJob Title - Director, Clinical Research, Immunology

Merck & Company IncCompany Name - Merck & Company Inc

•

Rahway, New Jersey, USA

Full-time

Job Description The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, the position may be responsible for: Evaluating pre-clinical and t

Senior Statistical ProgrammerJob Title - Senior Statistical Programmer

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

A senior statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. In this role, a typical day might include the following: The incumbent assi

Senior Manager, BiostatisticsJob Title - Senior Manager, Biostatistics

Sun Pharmaceutical Industries, Inc.Company Name - Sun Pharmaceutical Industries, Inc.

•

Princeton, New Jersey, USA

Full-time

Senior Manager, Biostatistics This position reports to the local area Lead within Biostatistics and Data Management (BDM) group at SPARC. The main responsibilities will include hands on day to day support of one or more clinical studies. The position will provide oversight of all statistical activities during lifecycle of the study. The main activities would include review of the Protocols, eCRF, SDTM/ADAM specs review, SAP authoring, DB lock support topline results validation/interpretation, C

Study Manager - CardiovascularJob Title - Study Manager - Cardiovascular

Merck & Company IncCompany Name - Merck & Company Inc

•

Rahway, New Jersey, USA

Full-time

Job Description This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for a single study or across multiple studies (e.g., operational

Manager, Statistical ProgrammingJob Title - Manager, Statistical Programming

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

As an integral part of a study, the statistical programmer provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. In this role, a typical day might include the following: Assist in providing mentorship in implementing and driving the programming and project standards. The evaluation and development of study requi

Principal Statistical ProgrammerJob Title - Principal Statistical Programmer

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, collaborators, and external functional service providers to ensure all the programming results are delivered in timel

Principal Scientist, Clinical Research, GYN MalignanciesJob Title - Principal Scientist, Clinical Research, GYN Malignancies

Merck & Company IncCompany Name - Merck & Company Inc

•

Rahway, New Jersey, USA

Full-time

Job Description Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork

Principal Scientist, Clinical Research, GYN MalignanciesJob Title - Principal Scientist, Clinical Research, GYN Malignancies

Merck & Company IncCompany Name - Merck & Company Inc

•

Rahway, New Jersey, USA

Full-time

Group Medical Director, Late Stage Oncology (Remote)Job Title - Group Medical Director, Late Stage Oncology (Remote)

AbbVieCompany Name - AbbVie

•

Jersey City, New Jersey, USA

Full-time

Job DescriptionJob DescriptionCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at .abbvie.com. Follow @ab

Senior Statistical ProgrammerJob Title - Senior Statistical Programmer

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

The Senior Statistical Programmer provides support to the lead programmer and study team on all programming activities according to the study requirements and the timelines. This role contributes to studies in various therapeutical areas and all clinical trial phases. The incumbent implements and executes the programming and project standard under minimal supervision of the lead programmer and manager to support ongoing clinical studies and requests for study report, regulatory submission, and a

Senior Statistical ProgrammerJob Title - Senior Statistical Programmer

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

Associate Director, Neuroscience Digital Health - NeurodegenerationJob Title - Associate Director, Neuroscience Digital Health - Neurodegeneration

Johnson & JohnsonCompany Name - Johnson & Johnson

•

Hopewell Township, New Jersey, USA

Full-time

Description Johnson & Johnson Innovative Medicine is currently seeking an Associate Director, Neuroscience Digital Health - Neurodegeneration to be located at one of our sites in Cambridge, MA, Titusville, NJ, or La Jolla, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our exp

Principal Scientist, Patient-Centered Endpoints & StrategyJob Title - Principal Scientist, Patient-Centered Endpoints & Strategy

Merck & Company IncCompany Name - Merck & Company Inc

•

Rahway, New Jersey, USA

Full-time

Job Description Under the general direction of the Patient-Centered Endpoints & Strategy (PaCES) group lead, the Principal Scientist has responsibility for supporting or co-leading global Clinical Outcomes Assessment (COA) endpoint strategies, including Patient-Reported Outcomes for specific disease areas. The individual will co-lead or guide teams on the development, validation, analysis and interpretation of COA endpoints to support regulatory submissions, reimbursement evidence dossiers, pay

Senior Medical Director, Late Stage Oncology-Product Safety Team Lead (Remote)Job Title - Senior Medical Director, Late Stage Oncology-Product Safety Team Lead (Remote)

AbbVieCompany Name - AbbVie

•

Jersey City, New Jersey, USA

Full-time

Sr. Specialist, User Acceptance Testing/Quality Control Analyst - HybridJob Title - Sr. Specialist, User Acceptance Testing/Quality Control Analyst - Hybrid

Merck & Company IncCompany Name - Merck & Company Inc

•

Rahway, New Jersey, USA

Full-time

Job Description Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. Responsibilities Responsible for developing, executing and coordinating the end-to-end Interactive Voice/Web Response System User Acceptance Testing.Responsible for the quality review of the URS a

Statistical ProgrammerJob Title - Statistical Programmer

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

The Statistical Programmer provides support to the lead programmer and the study team on all programming activities according to the study requirements and the timelines. The incumbent implements and performs the programming and project standard under general supervision of the lead programmer and manager to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. In this role, a typical day might include the following: Provide program

Director, Statistical Programming Medical AffairsJob Title - Director, Statistical Programming Medical Affairs

Regeneron PharmaceuticalCompany Name - Regeneron Pharmaceutical

•

Bernards, New Jersey, USA

Full-time

The Director of Statistical Programming Medical Affairs provides leadership to the group in Medical Affairs, including Health Economics and Outcomes Research (HEOR). The incumbent is responsible for activities related to statistical programming through multiple layers of management and senior-level staff. The role will own the effort across Medical Affairs projects to identify, initiate, develop, and implement programming standards, applications, processes, and training. In this role, a typical