It includes the opportunity to work with the executive directors to develop a strategic vision for the continued enhancement of adult services at PCDI. Reports to the Executive Director. ...
Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies, conduct hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clin...
Medical Directors of Oncology Clinical Research—Los Angeles. Tanner and Associates is recruiting several Medical Directors of Oncology Clinical Research for large Biotech companies located in San Francisco, Los Angeles, Salt Lake, and New Jersey. Major Biotech companies are seeking Medical Director/...
The Director, Clinical Safety, will be a product safety lead or part of a product safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-market...
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Ensure high quality standards, on time delivery within budget ...
Such trials could be pivotal for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO; Participates in creation of developmental and regulatory strategy; Drafts protocol profiles and sections of key submission documents; Point of contact for inter...
As the Senior Director of Clinical Data Management, you'll play a key role, responsible for being a hands-on DM leader across full lifecycle clinical development. Collaborate with clinical development team on strategies to improve data management quality and reporting efficiency. Develop eCRFs, reco...
Medical Director of Clinical Research. OneOncology’s non-exclusive clinical trial site management subsidiary, OneR, delivers complex, multi-center clinical trials to affiliated practices. The role requires a high-performing and energetic individual who demonstrates outstanding scientific knowledge a...
Provide strategic leadership and medical expertise within the Clinical Development neuropsychiatry and CNS space and deliver on developing, executing and advancing strategic and successful development programs for yourself and while providing mentorship and over to team members for their programs. S...
It includes the opportunity to work with the executive directors to develop a strategic vision for the continued enhancement of adult services at PCDI. Reports to the Executive Director. ...
The Hospice Director of Nursing is responsible for the oversight of nursing and aide services; coordinating the hospice team that includes social workers, spiritual and bereavement counselors, physicians, nurses and aides and overseeing the plan of care tor the hospice patients for a growing hospice...
The Director role in Tuberculosis (TB) is part of the Global Clinical Development team at Otsuka and reports to the Senior Director, Global Clinical Development, OPDC. You will provide clinical and scientific input as well as integrate in a variety of activities such as clinical operations, product ...
This position will play a crucial role in managing the import and export operations for Clinical Supply Chain Logistics (CSCL). The Associate Director, CSCL Customs & Trade Operations works in partnership with BMS Global Customs & Trade Compliance (C&TC) and closely with various other internal depar...
Experience in the pharmaceutical industry or in academic translational clinical research (as a general guideline, Director and 6-9 years for Senior Director levels is typically required depending on type of experience at application). While not essential, prior personnel management experience, will ...
As the Director/Senior Director of Clinical Development, you will be responsible for the following:. ...
The GRACS Global Process Lead (GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global business processes. ...
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...
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Requires 8-12 years experience in business development or sale...
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 Associate Director, Clinical Operations is responsible for Oversight of the Project Management team, Clinical Research Associates, Clinical Trial Associates as well as motivating, mentoring and training. Associate Director, Clinical Operations. Oversee and manage all operational aspects of phase...
Responsible for supporting Clinical Operations with overall management of the department’s clinical studies including project planning, clinical budgets, resource management and outsourcing management for assigned assets / therapeutic category unit. Acts as an integral resource for Clinical Operatio...
The Clinical Leader is a critical member of the Compound Development Team (CDT) which is dedicated to maximizing the value of the asset to patients and the company through the execution of all phases of clinical development and provides active medical and scientific contribution to cross-functional ...
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...
Experience in the pharmaceutical industry or in academic translational clinical research (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 years for Senior Director levels is typically required depending on type of experience at application). While not e...
We are seeking a talented Director of Clinical Research Consulting to join our exceptional Client Services Delivery Team. Vitalief thrives on identifying and recommending innovative ways of delivering services to our clients by providing Resourcing (staff augmentation), Management Consulting, and Ma...