- Merck & Co. (Rahway, NJ)
- …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. (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
- Merck & Co. (Rahway, NJ)
- …field and relevant experienceRequired Experience and Skills:-- -A deep understanding of the clinical trial process: You can speak the language of protocols, ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… 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
- Eisai, Inc (Nutley, NJ)
- …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
- 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 ... Medical Affairs department for assigned product(s). The Associate Medical Director utilizes expert medical, clinical and scientific knowledge in assigned… more
- Actalent (Parsippany Troy Hills, NJ)
- The Clinical Trial Assistant plays a crucial role in supporting clinical trial coordination and implementing clinical operational plans in line with ... + 3-5 years of experience in the biotech industry and clinical drug development or trial execution. + Advanced skills in Microsoft Office and knowledge of… more
- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
- Actalent (New York, NY)
- …Location of Candidate: Open to remote Candidates in EST Job Description Manage clinical trial activities for multiple trials, ensuring the timely completion of ... Job Title: Associate Director, Clinical Operations Company: Small...for assigned clinical trials. Responsibilities + Manage clinical trial activities for multiple trials, ensuring… more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- IQVIA (New York, NY)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Bristol Myers Squibb (Madison, NJ)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness + Represents DM… more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …responsible for abstracting medical record data and assigning codes using current clinical classification systems appropriate for the type of care provided. The ... the organizational structure to ensure proper code selection. Collaborates with clinical staff through written, verbal, or electronic clarification requests or… more
- Merck (Rahway, NJ)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills… more
- Pfizer (New York, NY)
- …+ Develop expertise navigating Pfizer compliance systems, registries (eg GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related to ... **JOB SUMMARY** + The overall role of the Early Clinical Research Clinician Associate Director is to...of clinical studies, and delivering on innovative clinical study designs, high quality trial execution,… more
- Merck (Rahway, NJ)
- …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 (Rahway, NJ)
- … 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 Research Group. Under the guidance of a supervisor, the… more
- Hackensack Meridian Health (Edison, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. Education, Knowledge, Skills and ... Preferred: + SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research… more
- Sanofi Group (Morristown, NJ)
- …progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team (CTT) and Project Team. This is a position for a ... **Job Title:** Associate Director-Principal Medical Writer **Location:** USA, Remote. Proximity...who has an extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership… more
- Merck (Rahway, NJ)
- …relevant experience **Required Experience and Skills:** + **A deep understanding of the clinical trial process:** You can speak the language of protocols, ... **Job Description** We are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… more
