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 ...
Associate Director, Clinical Data Management and Analytics. The Associate Director (AD), Clinical Data Management and Analytics will be responsible for evaluation of our Miltenyi Biomedicine US (MBM) data management practices to optimize our "hybrid" data management model. Our clinical research and ...
This position is responsible for the management and oversight of end to end clinical supply chain activity for assigned clinical protocols. This position works closely with key stake holders including Clinical Operations, Global Planning, Quality Assurance, Regulatory Affairs, Contract Manufacturing...
The Director, Clinical Project Management works cross-functionally with the Epidemiology, Biostatistics, Clinical Informatics, Engineering, and Data Science teams to drive the scoping and execution of new projects. We are a healthcare data and technology company focused on real world clinical data a...
Provides scientific and clinical input to study-related documents and analysis plans including informed consent forms, clinical research forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reports. The Clinical Development Associate Medical Director will serve...
Responsible for delivering clinical pharmacology components of clinical study protocols and clinical study reports. The Director, CPQP position resides within Alexion’s Clinical Pharmacology and Safety Sciences (CPSS) organization. As the CPQP lead, the incumbent is expected to provide subject matte...
Provides scientific and clinical input to study-related documents and analysis plans including informed consent forms, clinical research forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reports. The Associate Medical Director will serve as the Medical Lead ...
As Senior Director, Clinical Operations, you will be accountable for overseeing a Clinical Operations team that will lead the industry in speed and quality of clinical study design and execution. You will partner with Clinical Operational Excellence to oversee the development and maintenance of clin...
Provides scientific and clinical input to study-related documents and analysis plans including informed consent forms, clinical research forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reports. The Clinical Development Associate Medical Director will serve...
Reporting to the Senior Director, Clinical Data Management, the Associate Director, Clinical Data Management will define and lead the clinical data management strategy for the organization. ASSOCIATE DIRECTOR CLINICAL DATA MANAGEMENT. The Associate Director, Clinical Data Management is responsible f...
Provide 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). You will work on multiple clini...
The Director of Clinical Research will report to the Chief Clinical Officer and will collaborate with internal teams and external partners to elevate the scientific profile of our company and contribute to the broader field of digital behavioral health. InStride Health is seeking a Director of Clini...
The Clinical Research Director (CRD), Amlitelimab, Immunology and Inflammation Therapeutic Area, for the integrated evidence generation plan (IEPG) is responsible for the strategy, development, execution and reporting of key data generation activities (e. Understands and keeps updated with the pre-c...
The Director, Clinical Operations is a leadership role responsible for overseeing and managing all aspects of clinical operations for a high priority immunology program. This individual possesses clinical operations expertise with a track record of success, working with peers and stakeholders across...
The Director, Clinical Quality within Research & Clinical Development Quality Assurance will be responsible for the oversight and support of the Sarepta Clinical Development and Real World Evidence portfolio. This position will be a core member of the Clinical Trial team and provide Clinical Trial t...
DIRECTOR OF CLINICAL SPORTS PSYCHOLOGY & ATHLETE WELLNESS,, Student Health Services. The director performs a wide range of complex tasks including coordinating the clinical treatment team of mental health providers which delivers group, individual and athletic team services for all BU student-athlet...
The Clinical development department is responsible for the medical aspects of development activities, including clinical development plans (CDP) and clinical trials. The Associate Medical Director will contribute to the direction, planning, execution, and medical oversight of clinical trials and ali...
Reporting to the Senior Director, GCO, Patient and Site Engagement, the Director, Clinical Trial Liaison must have an in-depth understanding of clinical research and associated regulatory requirements and lead the Site Engagement team and have specific therapeutic & operational expertise in mult...
The purpose of the Senior Director of Clinical Research role is to coordinate and lead the development of first in man (FIH), proof of mechanism (POM), proof of clinical activity (SoCA) and proof of concept (PoC) and dose ranging studies for novel biological and small molecule therapies in. Provide ...
The Regional Director of Clinical Services will be responsible for providing clinical oversight, mentorship, and guidance to the Directors of Nursing at each facility. Regional Director of Clinical Services. Regional Director of Clinical Services. This is an exciting leadership opportunity for a sea...
Perform quality review checks on key clinical documents such as clinical protocols, informed consent forms, case report forms, clinical monitoring plan, monitoring reports, etc. The sponsor oversight monitoring role plays a significant contribution to the clinical quality risk management strategy fo...
The Medical Director may lead a cross functional team in the design and execution of a clinical. May supervise and develop Medical Directors and CDS in preparation of clinical. Engage with clinical investigators nonclinical studies to enable quality. The job holder supports assigned clinical develop...
Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements,...
Lead the development of contingency/risk management plans for projects and assist Director/Senior Director of Clinical Operations in the preparation and execution of sound development strategies. Associate Director, Clinical Operations(. Provide strategic input and execution of clinical trials from ...
Oversee investigator-initiated and grant funded clinical trials including development of protocols/budgets, support the contract process, and coordinate correlative sample processing Lead process improvement projects to increase accrual and study approval/activation timelines Lead process improvemen...