- Merck & Co. (Rahway, NJ)
- …costs, executing contracts and ongoing contract management. This role will report to the Associate Director, Clinical Trial Central Labs to support high ... support for Clinical Development Sourcing and Procurement (CDSP) in Clinical Trial Central Labs. This includes sourcing of clinical services utilizing… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …manage trial progress. Medical Monitoring: Provide medical oversight during clinical trials to ensure participant safety and data integrity.Review and interpret ... OverviewThe Respiratory Clinical Development Medical Lead will oversee the clinical and medical aspects of new respiratory medicines, including new drug or… more
- Merck & Co. (Boston, MA)
- …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Merck & Co. (Upper Gwynedd, PA)
- … Clinical Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, ... serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical ...an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- Genmab (NJ)
- …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Merck & Co. (North Wales, PA)
- …Engineering or closely related field plus 9 years SAS programming experience in a clinical trial environmentOR a Master's degree (or US equivalent) in Computer ... closely related field plus 7 years SAS programming experience in a clinical trial environment.Requirements:Experience and knowledge in leading large and/or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and globally, and provide legal support for licensing, co-promotion, co-development, clinical trial collaboration, co-marketing and acquisition agreements (among ... in negotiating, drafting and reviewing licensing, co-promotion, co-development, co-marketing, clinical trial collaboration, companion diagnostic, and acquisition… more
- Insmed Incorporated (Minneapolis, MN)
- …strong related experience.Other Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical ... for the future of science, we're in. Are you?About the Role:The Associate Director Medical Science Liaison will develop and maintain professional relationships with… more
- Eisai, Inc (Cincinnati, OH)
- …and other international regulatory/ethical guidelines relevant to the pharmaceutical industry & clinical trial conduct, and to ensure compliance with these ... 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… more
- Insmed Incorporated (San Diego, CA)
- …automation, development of custom tools, and data exchange solutions that enhance clinical trial efficiency.Solid understanding of CDISC standards (CDASH, SDTM) ... future of science, we're in. Are you?About the Role:The Associate Director, EDC Programming will lead and oversee EDC...and oversee EDC programming, and database build for in-house clinical trials. This role will be responsible for the… more
- Insmed Incorporated (NJ)
- … Director of Biostatistics is responsible for the statistical aspects for complex clinical trial (s) or indication product line. This role leads the protocol ... statistical section development, study setup, execution, analysis, and reporting of clinical trials, and interacts with cross-functional teams.What You'll Do: Lead… more
- Insmed Incorporated (St. Louis, MO)
- …and infectious diseaseOther Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical ... a local medical and scientific resource to Insmed for product planning, clinical insights, and intelligence. Collect, synthesize and deliver HCP derived scientific… more
- Eisai, Inc (Nutley, NJ)
- …country strategic development, planning, implementation, and oversight of Phase I through IV clinical trial programs and early new product development within the ... therapeutic area.Under the direction of the Vice President, Medical Affairs the Associate Medical Director is responsible for working with key stakeholders to… more
- Insmed Incorporated (NJ)
- …the advancement of innovative statistical methodologies.Hands-on experience in designing and analyzing clinical trial data, with proficiency in SDTM and ADaM ... statistician to join our dynamic Biometrics Medical Affairs team. The Associate Director of Medical Affairs Biostatistics is responsible for the statistical… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for ... and primary point of accountability and reconciliation for the Trial Master File (TMF) and the Investigator Site File...resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or… more
- Caris Life Sciences (Phoenix, AZ)
- …yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist-Biorepository provides operational and regulatory support for ... + Candidates should have 1-2 years' experience in a Biorepository setting or Clinical Trial setting + Proficient in Microsoft Office Suite, specifically Word,… more
- Translational Research in Oncology (Los Angeles, CA)
- … research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing ... If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO… more
- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …basis. Qualifications Required Education and Experience: 2+ year of experience in clinical trial research is required (preferred in medical devices). Advanced ... pharmacy/ nursing desired. Skills and Abilities Required for This Job: Proficient in clinical trial management and electronic data capture systems to document… more
