Use medical and clinical expertise in design, implementation and monitoring of clinical studies (from Phase 1 to 4) in a team setting. Reports to the Executive Director- Clinical Research & Development. Write and/or review clinical sections of clinical trial reports, statistical reports, investi...
Associate Director, Clinical Operations Sun Pharma Advanced Research Company Limited Princeton, New Jersey SummaryThe Associate Director, Clinical Operations is responsible for Oversight of the Project Management team, Clinical Research Associates, Clinical Trial Associates as well as motivating, me...
The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. The CP&P team interacts with discovery and translational scientists, project leadership, earl...
Associate Director, Clinical Operations Sun Pharma Advanced Research Company Limited Princeton, New Jersey SummaryThe Associate Director, Clinical Operations is responsible for Oversight of the Project Management team, Clinical Research Associates, Clinical Trial Associates as well as motivating, me...
Study outputs: Draft responses to IRBs and Health Authorities; Collaborates with Translational Medicine and Clinical Pharmacology to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with Delivery...
We have an immediate opening in our Monmouth Junction, NJ facility for an experienced MD to serve as Senior Director or Director, Clinical Development. The position is a core member of the Clinical Development management team responsible for developing and implementing, in alignment with corporate s...
Trains all new clinical employees within their scope and coordinates training with clinical team members. Supports Executive Director with 90-day, annual performance reviews, and growth plans for therapists within the program, as requested by the Executive Director. Oversees and ensures quality of c...
Provides senior-level clinical representation at meetings with health authorities; leads the creation of developmental and regulatory strategy; accountable for performance of CROs; routine interactions with senior management of CRO/ARO, as needed; accountable for clinical development plans, protocol...
The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. The Associate Director Clinical Sciences leads in the development, evaluation, p...
The Director, Clinical Operations will serve as the primary contact for the contract research organizations (CROs), laboratory vendors and clinical sites involved in the clinical trials. The Director, Clinical Operations will provide operational and implementation expertise to the project teams unde...
The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. The CP&P team interacts with discovery and translational scientists, project leadership, early and la...
Proclinical is seeking a dedicated and innovative Executive Director to head up the department of Global Clinical Quality Assurance. Executive Director of Global Clinical Quality Assurance - Permanent - NJ. Executive Director of Global Clinical QA's. Collaborate with regulatory affairs and clinical ...
The Director of Nursing is responsible for the direction, provision, and quality of nursing services for the hospice program. The Director of Nursing must be available at all times during the operating hours of the agency. The Director of Nursing reports to and receives consultation, direction and s...
You will ensure that Agilent’s processes for clinical quality oversight of clinical trial conduct, clinical trial sites, and suppliers, as well as vigilance oversight of product quality issues are robust and in alignment with ICH E6, other applicable Good Clinical Practice (GCP) and Good Vigilance P...
The Director, Clinical Research Collaborations Lead, will co-lead cross-functional efforts focused on creating an optimal engine for identifying, ideating, and actively sourcing research concepts that will address critical evidence gaps for BMS’s Immunology, Cardiovascular and Neuroscience\Neuro-psy...
Key Skills:</p><ul><li>Experience leading and managing complex global clinical development programs is required</li><li>Superior verbal, written, and presentation communication skills in relating to colleagues and associates both inside and outside the organization</...
This position serves as a key role in the effective implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various stages of clinical development (including clinical trial implementation, and oversight of...
Use medical and clinical expertise in design, implementation and monitoring of clinical studies (from Phase 1 to 4) in a team setting. Reports to the Executive Director- Clinical Research & Development. Clinical study management: Provide regional medical & scientific input on trial outlines, trial p...
The Director, CRC Lead, Hematology/Cell Therapy, will co-lead cross-functional efforts focused on creating an optimal engine for identifying, ideating, and actively sourcing clinical research collaborations that will address critical evidence gaps for BMS’s Hematology/Cell Therapy assets. The Medica...
The Clinical Director is responsible for the supervision and clinical oversight of the program. Trains all new clinical employees within their scope and coordinates training with clinical team members. Supports Executive Director with 90-day, annual performance reviews, and growth plans for therapis...
The Director Clinical Development is the clinical/medical/scientific expert who supports the translation of a target product profile into a feasible Clinical Development Plan (CDP), taking into account scientific environment, resource possibilities, clinical feasibility and timely execution. Provide...
Interacts with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials, as well as ensure the clinical program is appropriately designed. Director, Biostatistics Ea...
Use medical and clinical expertise in design, implementation and monitoring of clinical studies (from Phase 1 to 4) in a team setting. Reports to the Executive Director- Clinical Research & Development. Write and/or review clinical sections of clinical trial reports, statistical reports, investi...
The Director will work closely with senior management and our business development team to gain credibility with our clients by identifying and recommending innovative ways of delivering services to our clients by providing Resourcing Services, Consulting Services, Managed Services, and Learni...
Job Title: Associate Director, Clinical Safety MD. Provides integrated safety input into all safety relevant parts of regulatory documents (IB, CCDS, RMP, REMS, DSUR, PSUR, CSR, Clinical Overview and Integrate safety summary) required during active development, and submission phase. Pharmacovigilanc...