- Merck & Co. (Rahway, NJ)
- …Description: This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) ... and Monitoring, the person is responsible to manage a team of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study and site performance with… more
- Merck & Co. (Rahway, NJ)
- …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Respiratory will focus on driving strategy, development, and ... those new to the organization therefore requiring someone who has built and lead clinical development plans from the ground up. They will also be responsible for… more
- Merck & Co. (North Wales, PA)
- …the Research & Division organization of our company.- Position Description/Summary: The GPAM Associate Director, Project Manager, is a core member of Early Drug ... progress the Research & Development pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and… more
- Merck & Co. (North Wales, PA)
- …biomarker project management and operational expertise to support cross-functional clinical teams, ensuring the timely and efficient delivery of the biomarker ... aspects of each study.This position will report into the Associate Principal Scientist of Project Management and...clinical biomarker assay execution and demonstrated success in project management. As a key contributor to the … more
- Merck & Co. (Rahway, NJ)
- … Clinical Development Finance Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist will:Provide ... for a wide range of stakeholders including the Global Project Manager, Alliance Manager, Global Trial Manager, Clinical...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …for clinical trial projects (data, analyses, tables, graphics, listings)Strong project management skills; leadership at a program level; determines approach and ... potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality… 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
- Merck & Co. (North Wales, PA)
- …programming analyst will be a key collaborator with modelers, statisticians and other project stakeholders and is expected to execute project plans efficiently ... when opportunities arise. Primary Activities :Programmatically synthesize preclinical / clinical data into analysis ready structures from varied data sourcesCreate… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description The Associate Director, Technical Operations within Global Clinical Supply (GCS) is responsible for managing all aspects of ... equipment/facility project activities, and supporting infrastructure-related projects to establish, upgrade, and modernize Clinical Supply Operations (CSO)… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs… more
- Merck & Co. (North Wales, PA)
- Job DescriptionWe are currently recruiting for the position of Associate Director, US Oncology - Hematology Scientific Strategy. This talented individual will lead ... a robust scientific leader (SL) engagement plan, coordinating with medical affairs, clinical research, and global marketing to provide a consistent One our Company's… more
- Merck & Co. (Rahway, NJ)
- …risk management techniques to positively support and influence clinical and commercial combination product development and launches.Principal ResponsibilitiesLead ... ensure full integration of the device development activities with the clinical , regulatory, formulation, commercial and other key company functions.Represent Device… more
- Merck & Co. (Rahway, NJ)
- …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... fast-paced job that provides a high degree of technical, project , and people management responsibility. - This SSO Facility...members to ensure the quality and safe delivery of clinical supplies, the scientific rigor of the processes, and… more
- Merck & Co. (North Wales, PA)
- …processes) including experience including bringing materials through legal, regulatory, and clinical review Strong project management skills as demonstrated by ... of the role Preferred Experience and Skills: Ability to translate science/ clinical data into clear marketing strategies, medical education and/or conference… more
- Merck & Co. (North Wales, PA)
- …talented and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist) has primary responsibility for the planning ... and directing clinical research activities involving new Oncology medicines within an...capitalize on opportunities to adapt direction in light of project successes and failures and market changes.--Managing selected opportunities,… more
- Merck & Co. (Rahway, NJ)
- …will be directly responsible for a team of approximately 10-15 senior and associate level scientists in Rahway, New Jersey. -The position is accountable for ... and effective prioritization to bring analytical representation and expertise to project teams and support regulatory filings (eg, INDs/IMPDs and BLAs).-The Director… more
- Aequor (Thousand Oaks, CA)
- Description 3 year contract 100% remote Shift/Schedule: 8:00 -4:30 pm (flex) -Monday - Friday **Candidates must have GMP and pharmaceutical experience** What you ... to the Product Quality (PQ) organization as a subject matter expert of clinical and commercial product stability studies and GMP data management. In this team-based… more
- Fresenius Medical Center (Meriden, CT)
- …of the Project Assistant is to provide support to the members of the clinical project team, in order to facilitate management of clinical trials. The ... utilizes databases and programs as deemed necessary. + Maintains clinical project files to internal standards and regulatory requirements. + Contributes… more
- Merck (Columbus, OH)
- …**Position Description:** This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) ... person is responsible to manage a team of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study...a team environment + Excellent people management, time management, project management and organizational skills + History of strong… more
