- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team...Responsibilities Study Strategy: Provides the strategic direction to Biostats Data Mgmt & Data Ops for EDC,… more
- Merck & Co. (Rahway, NJ)
- …set up)Lead medical monitoring team in review and interpretation of clinical data /medical protocol-deviations in collaboration with the Clinical ... Job DescriptionPosition Description: Associate Director, Clinical Scientist This position...Program Lead, you will collaborate with global, cross -functional team members including clinical directors and study… 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
- Merck & Co. (Rahway, NJ)
- …or health care related discipline.Required Experience and Skills:At least 8 years working on a clinical trial team or has worked in a clinical operations ... 10%Flexible Work Arrangements:Not ApplicableShift:1st - DayValid Driving License:NoHazardous Material(s):NoRequired Skills: Clinical Trials, Dashboard Reporting, Data Literacy, Metrics… more
- Merck & Co. (Rahway, NJ)
- … clinical data repository from external biomarker vendors. Work with Clinical team and/or Central labs to design sample collection kits, laboratory ... candidate will work closely with Biomarker leads, Assay scientists, Vendor Managers and Clinical team to ensure that critical timelines are meet by our… more
- Merck & Co. (Rahway, NJ)
- …and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the ... The Associate Principal Programmer will write programs to analyze data with statistical methods which are not currently available through commercial software… more
- Merck & Co. (North Wales, PA)
- …other team members when opportunities arise.Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …you ready to make a difference? The Position Reporting to the head of Clinical , medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR… more
- Merck & Co. (North Wales, PA)
- …and high-quality data to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports the ... of patients and global human health. Our Quantitative Sciences team uses big data to analyze the...Specific Required Skills and Experience:Significant expertise in SAS and clinical trial programming including data steps, procedures,… 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
