The Assistant Director of Adult Clinical Services is responsible for assisting the Director of Adult Services in the day-to-day operation of the clinical services and implementation and monitoring of all behavioral programming. In addition, the Assistant Director of Adult Clinical Services assists t...
MASTERS REQUIRED** The Clinical Director is responsible for the management and quality assurance of all clinical services provided by the Company including the training and supervision of all clinical staff. The Clinical Director works closely with the Executive Director to drive a program developme...
The Senior Medical Director, Clinical Development will play a key role in the NASH/MASH clinical development program within the Regeneron Genetic Medicines portfolio, including responsibility for driving forward one or more NASH/MASH clinical programs. This role leads one or more clinical team worki...
The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. Applies clinical/medical decision making to clinical development issues...
This role will report to the Head of Clinical Development in Oncology, for Moderna and have direct medical responsibility for the clinical development programs including creating overall clinical development plans, designing clinical studies, writing protocols, ensuring timely execution and medical ...
A seasoned clinical operations professional who enjoys performing the day-to-day tasks of clinical operations but also has the knowledge and experience to build out the end-to-end clinical capabilities of a developing clinical research organization. Director/Senior Director of Clinical Operations. A...
Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate. Provide oversight and mentorship to assigned Clinical Trial Managers and Clinical Tria...
We are constantly looking to add to our core talent.If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further - Haemonetics is your employer of choice.Check below to see if you have what is needed for this opportunity, and if so, m...
The Associate Medical Director (AMD), under the direction of the Director of the Office of Clinical Affairs (OCA) or his/her designee, is responsible for providing clinical expertise to OCA and EOHHS program staff. Provide clinical leadership and mentoring for the OCA and MassHealth staff and work c...
Clinical Science deliverables for clinical trials and programs associated with the clinical development of molecules in the stages of clinical development (Phase I – III). Associate Director, Clinical Science. Associate Director, Clinical Science. Associate Director, Clinical Science. ...
Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR). The Associate Medical Director ...
The Clinical Program Director will have a variety of roles and responsibilities within the JTS program including but not limited to supervising case managers and managing a caseload of tenants, providing clinical feedback and consultation to staff regarding clients that have complex mental health ne...
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REQUIRED: doctorate in clinical or counseling psychology from an American Psychological Association (APA)-approved doctoral program; completion of APA-approved clinical internship or its equivalent; Massachusetts licensure or license eligible; at least five years of supervised clinical internship/fe...
The Senior Clinical Scientist reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs. May support clinical development planning (collaboration with Clinical Development Lead/Clinical Trial Physician for provisio...
In addition, you will serve as the liaison for all clinical-scientific aspects of a trial within the study team and provide clinical science expertise within preclinical projects. Director, Clinical Science Lead. The Clinical Science Lead is a key figure for leading the clinical science perspective ...
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...
Assistant Clinical Director-(3295857). In conjunction with the clinical director, provides corrective action (as needed). Attends meetings on behalf of Clinical Director when needed. Supervises clinical managers and educators within area(s) of oversight. ...
Provide expert leadership to deliver submission communication strategies and drive the authoring of large clinical submission packages and other complex clinical documents that are aligned with project development plans, regulatory requirements, and communications best practices. Create robust clini...
The CL will apply deep medical and clinical knowledge to translate clinical research ideas into high-quality decision-making data, working closely with subject matter experts from statistics, clinical pharmacology, and other team members. The Clinical Lead (CL), Internal Medicine RU (IMRU) will be t...
Reporting to the Head of Clinical Supply Chain, the Associate Director of Clinical Supply Planning will focus on managing and optimizing global supplies to ensure timely availability of clinical supplies for clinical trials. This is a critical role that will also be involved in setting up a robust c...
Support preparation of scientific material for conference presentations or publications Contribute to the authoring and revision of regulatory submissions Perform analyses and generate scientific slide decks based on clinical, translational and other datasets Minimum Qualifications PhD, RN, or NP wi...
The Director, Strategic Project Management - Clinical Development and Safety is a pivotal role that offers strategic project management expertise to support the Clinical Development and Safety team. The Director will also play a key role in developing and driving the Clinical Development Plan (CDP) ...
As the Director of Clinical Operations at Foghorn, you will play a pivotal role in driving the success of critical clinical programs. You'll provide strategic leadership and operational expertise to guide our Clinical Development team, ensuring the seamless execution of clinical trials. Director of ...
Director, Clinical and Quantitative Pharmacology will combine strong pharmacometric skills with a deep biological understanding. The Director determines, plans, and executes technically challenging analyses by using state of the art Modeling & Simulation methodologies to strongly contribute to c...