Minimum of three years' clinical outpatient experience and two years' clinical supervision or clinical program development experience preferred. The Physical Therapist Clinical Director is responsible for complete oversight of operations and administration of rehabilitative outpatient clinic...
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 Director, Clinical Operations/CPM is responsible for the development of a Clinical Operations Team in the United States. Director, Clinical Operations/CPM. Team Mentoring, Motivating, Training and Oversight for a team of Project Managers, Clinical Research Associates (CRAs), Clinical Trial Assoc...
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...
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 global head of regulated bioanalysis will also form strategic internal (DMPRL, Clinical Operations, Data Management, Scientific Operations…etc) and external partnerships to achieve the objectives of the global regulated bioanalysis group. This position has extensive knowledge of regulated BA, DM...
Minimum of three years' clinical outpatient experience and two years' clinical supervision or clinical program development experience preferred. The Physical Therapist Clinical Director is responsible for complete oversight of operations and administration of rehabilitative outpatient clinic providi...
Ensure that adequate (Oncology) Clinical Science resources are deployed to clinical studies from end to end in collaboration with GCLs, Physician Scientists and the study team (data management, clinical operation and other functions) to implement clinical development plan: study ideation, protocol d...
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...
Provide appropriate medical input & clinical leadership for all activities related to study conduct such as responses to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the Centralized monitoring, clinical and medical information for the st...
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...
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...
Director, Clinical Operations/CPMSun Pharma Advanced Research Company, Limited SummaryThe Director, Clinical Operations/CPM is responsible for the development of a Clinical Operations Team in the United States. Responsibilities Assigned:Team Mentoring, Motivating, Training and Oversight for a team ...
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...
Working with early- and/or late-stage clinical development teams, he/she will have the opportunity to drive translational research and clinical biomarker development for critical oncology clinical programs. Hypothesis-building & strategy forming: collaborate with stakeholders in clinical development...
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...
As Associate Director Global Clinical Trial Manager (GCTM) in Clinical Operations at Genmab, you will be part of the Trial Management team, currently more than 75 highly motivated and experienced people located in Denmark, the United States, the Netherlands, and Japan. Minimum 5 years of experience ...
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...
Leadership of the early clinical development strategy for novel therapy programs from preclinical candidates through initial clinical testing (Phase 1) and clinical Proof-of-Concept (Phase 2). Development and execution of early clinical strategy for novel therapeutics including authoring initial cli...
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 Associate Director, Clinical Imaging will own the strategy and execution of sophisticated early and late phase oncology imaging in clinical trials where imaging plays a meaningful role. We assume you will be an imaging scientific leader and a member of cross-functional program teams including Re...
The Director, Clinical Operations/CPM is responsible for the development of a Clinical Operations Team in the United States. Director, Clinical Operations/CPM. Team Mentoring, Motivating, Training and Oversight for a team of Project Managers, Clinical Research Associates (CRAs), Clinical Trial Assoc...
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...
Designs and develops clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical phar...
As part of our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director, USMA Solid Tumor Portfolio. Provides US market input to Global clinical development and Global Medical Affairs programs, staying abreast of the evolving scientific & competitive landscape for relevant solid...