- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Leadership:Has primary accountability for operational study-level timeline, cost, and quality deliverables. Lead the development of the clinical study plan ... including critical path activities and interdependencies for assigned clinical stud(ies) utilizing Microsoft Project or equivalent. Lead the creation of the cross… more
- Merck & Co. (Rahway, NJ)
- …including those new to the organization therefore requiring someone who has built and lead clinical development plans from the ground up. They will also be ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Rahway, NJ)
- …Distinguished Scientist (Executive Director) and Product Development Team (PDT) lead , Oncology Global Clinical Development, has primary responsibility ... the field of breast cancer. The Executive Director, PDT lead will manage the entire cycle of clinical...clinical studies.--Will report and work collaboratively with the- Associate Vice President to promote the development strategy of… more
- Merck & Co. (Rahway, NJ)
- …IMPDs, NDAs, BLAs, etc.) for combination product programs under your leadership. Lead /support/oversee clinical supplies production with respect to device ... to achieve safe and effective delivery to their intended site of action.- The DPPD Team manages the development...to set tactical and strategic direction on programs they lead to ensure high quality products and robust manufacturing… more
- Merck & Co. (Rahway, NJ)
- …and manufacturing to manage clinical development projects Assist the Associate Vice-President/Vice-President and product development team lead in ensuring ... Job DescriptionThe Executive Clinical Director (Distinguished Principal Scientist) has primary responsibility...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… 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
- Genmab (NJ)
- …other cross-functions to provide high-quality and timely deliverablesResponsibilities Lead or co- lead one or more complex clinical trial(s) in a therapeutic ... global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or...other key data management deliverables (eg database lock activities). Lead the development of medical data review plan (MDRP),… more
- Merck & Co. (North Wales, PA)
- …for Product Manager - PV Case Intake and Processing. Reporting into Product Line Lead Patient Safety and Quality & Compliance, this position will be responsible for ... and integrity.-Collaborate with other departments: Collaborate with departments such as clinical , regulatory, and safety to ensure that PV processes are integrated… more
- Merck & Co. (Boston, MA)
- …Bioanalytics (PDMB) group is seeking a dynamic, strategic thinking and collaborative Associate Principal Scientist to contribute to our small molecule and peptide ... drug discovery and early clinical development efforts. -This position will be based at...research labs in Boston, MA.- The ideal candidate will lead drug metabolism and pharmacokinetic (DMPK) efforts as a… 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. (Lower Gwynedd, PA)
- …Us: The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late ... IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data.… more
- Genmab (Plainsboro, NJ)
- …to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be responsible for leading the development and ... and Intelligence. The position will be based in our Princeton, New Jersey site which requires onsite presence 60% of the time per our hybrid… more
- Merck & Co. (Rahway, NJ)
- …and execution of scientific & medical affairs plans for Ophthalmology). They build and lead a team of TA dedicated global and regional directors and associate ... Global Brand and V&I Outcomes Research leads to define clinical development plans and brand strategies for assigned TAsProvides...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Rahway, NJ)
- …Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team that will build biopharmaceutics ... stakeholders across organizations such as Regulatory CMC, formulation functions, and clinical functions to ensure timebound progression of portfolio, initiatives for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of medical coding services for assigned programs, collaborating with program teams, clinical safety and pharmacovigilance, CROs, and partners to ensure high quality ... disciplines and cultures. This position requires a demonstrated ability to manage/ lead people and a variety of projects concurrently. Additionally, this position… more
- Lilly (IN)
- …The anticipated wage for this position is $111,000 - $162,800 **Job Description** The Clinical Research Lead (CRL) is responsible for the management of ... / site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives and delivery of database… more
- AbbVie (North Chicago, IL)
- …Conceives, executes and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial ... proposals and leads those efforts. Anticipates and critically evaluates Clinical Pharmacology, PK/PD or regulatory advances, strengths, weaknesses, opportunities and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …primary accountability for operational study-level timeline, cost, and quality deliverables. + Lead the development of the clinical study plan including critical ... for assigned clinical stud(ies) utilizing Microsoft Project or equivalent. + Lead the creation of the cross functional Clinical Study Oversight Plan… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director, Global Clinical Quality Date: Jan 7, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... and regulations, supports risk management activities, and leads continuous improvement for clinical development activities. The Associate Director - Global … more
- UCLA Health (Inglewood, CA)
- …of a multidisciplinary team, the clinical site director will serve as the clinical lead for two sites in a dyad relationship with the site manager. ... the leadership of the Chief Medical Officer, the Inglewood Site Clinical Director provides the majority of...service delivery systems within their site . The site director reports to the Associate Medical… more
