- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director, Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 ... Program Lead, you will collaborate with global, cross -functional team members including clinical directors and study managers to lead/support clinical -trial… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit ... Authorization Applications (MAAs), and local country submissions. Collaborates with PSL/ Clinical Safety Physician(s) and cross-functional team to develop… more
- Novo Nordisk Inc. (Los Angeles, CA)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability;...(subset of) NACD and/or as part of a global team and as aligned to a business case, goals… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant ... this position works with other CSPV staff and cross functional Safety Management Team (SMT) members, often handling straight-forward CSPV tasks such as single event… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …site identification activities in collaboration with the CRO and the study team . Oversee the site qualification process.Monitor clinical trial performance and ... primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy....stud(ies).If assigned, Sr. CSM may act as the Study Team Leader for the assigned clinical study… more
- Merck & Co. (Rahway, NJ)
- …candidate will work closely with Biomarker leads, Assay scientists, Vendor Managers and Clinical team to ensure that critical timelines are meet by our ... of each study. This position will report into the Associate Principal Scientist of Project Management. You will have... data repository from external biomarker vendors. Work with Clinical team and/or Central labs to design… more
- Merck & Co. (Rahway, NJ)
- …Steatohepatitis (MASH).The individual will be responsible for overseeing Product Development Team Leaders and- Clinical Directors within their group to ensure ... Job DescriptionThe Associate Vice President (AVP)/ Metabolism Section Head in...in the Atherosclerosis & Metabolism Therapeutic Area within Global Clinical Development will focus on driving strategy, development, and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In BARDS (Biostatistics and Research Decision Sciences), a ... programming analysis and reporting deliverables for global stakeholders. The Associate Principal Programmer will gather and interpret user requirements for… more
- Merck & Co. (Rahway, NJ)
- …validation of Mass Spectrometry based assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position ... (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all...is seeking a highly motivated candidate to join our team . The individual will play a critical role in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and external ... and posters/oral presentations that report results from our company's General Medicine clinical trial program, as well as select early-stage development projects and… more
- Merck & Co. (North Wales, PA)
- …these analyses.Prepares oral and written reports to effectively communicate results of clinical trials to the project team , company Management, regulatory ... for related drug/vaccine projects in Late Development Statistics.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and other company… more
- Eisai, Inc (Baltimore, MD)
- …If this is your profile, we want to hear from you. The Associate Director/Director, MSLs is responsible for the leadership, direction and management of MSLs ... with strategic and tactical planning, working collaboratively with Medical Affairs and Clinical Development teams for support of clinical studies across the… more
- Merck & Co. (North Wales, PA)
- …statistical-analysis and high-quality data to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports ... of patients and global human health. Our Quantitative Sciences team uses big data to analyze the safety and...or more years of SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (Rahway, NJ)
- …testing nodes in support of clinical and PPQ supplies. Additionally, the Associate Director leads, manages, and develops a team responsible for providing ... Job DescriptionThe Associate Director of Method Development & Testing is...clinical and PPQ supplies.Lead, manage, and develop a team responsible for providing routine functional testing support for… more
- Merck & Co. (Rahway, NJ)
- …company's biologics pipeline. We work closely with colleagues in Discovery, Pre- clinical and Early Development to rapidly develop manufacturing processes for diverse ... biotherapeutics, and efficiently manufacture material to supply clinical trials. We are also responsible for commercial process development and the development and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Associate Director of Quality Project Management and Strategyas part of the Quality team based in Raritan, NJ. Role OverviewThe Associate Director of Quality ... improvement projects within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Merck & Co. (North Wales, PA)
- … team members when opportunities arise.Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from varied data ... or related field plus 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
