Lead Clinical Trial Operations Manager Jobs in Hudsonville, MI

The official title for this role will be Regional Project Lead.The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by More...

The Senior Manager Regulatory Affairs US Advertising and Promotion ImmunologyDermatology combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual deve More...

Responsibilities: The ideal candidate is a selfstarter and team player with a strong desire to learn and grow in the field. Reporting to the Head of Data Management this position will be responsible for the implementation maintenance and coordination of clinical data management activ More...

We are looking for an experienced Associate Director Corporate Development to be responsible for a wide range of strategic finance activities.  Youll play a critical role on Privias finance team in an exciting growth phase of the company.  Youll develop a deep understanding More...

As the Field Medical Strategy & Insights Lead within the Global Medical Affairs (GMA) organization you will spearhead the development of an overarching strategy for the Global Field Medical Team (MSLs) to support clinical trials site engagement scientific exchange and insights gat More...

About This RoleThe Medical Director Lupus role is a part of Immunology Specialty Care North America (US) Medical a strategic partner within Biogen that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. As a key member of t More...

The Senior Director of Regulatory Affairs ensures that all divisions comply with applicable federal state and provincial laws and regulations maintaining continuous operating approvals. This role also leads efforts to develop and influence regulatory policies impacting the delivery of More...

About This Role:As a Medical Director Clinical Development Immunology you will be an integral member of the Immunology Therapeutic Area within the Clinical Development Organization. In this dynamic role you will play a critical part in shaping and advancing clinical programs particula More...

About This Role:As a Senior Medical Director for Alzheimers disease & Dementia (ADD) Clinical Development you will be at the helm of pioneering programs that have the potential to transform lives. Youll lead and oversee clinical development activities across both early and latesta More...

As a member of the Corporate Development team the Director Corporate Development and Mergers & Acquisitions North America supports the development and overall external growth strategy of SGS in the North America (US and Canada). They work closely with business and regional teams t More...

The Director of Medical Engagement Excellence Oncology reports to the Senior Director of Medical Affairs Operations.  The Director of Medical Engagement Excellence is responsible for leading all aspects of medical training for field teams to uphold the highest standards of medic More...

The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.Acts as primary communication point for project teams and company departments regarding clinical data managementActs as primary communication point for clients/vendors More...

The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. The Manager has the responsibility for 12 of the following: the More...

*Employee can work remotely anywhere in the U.S.  The Principal Medical Writer is responsible for providing writing support and advanced scientific writing expertise to the teams ensuring successful preparation of high quality documents and effective implementation of the wr More...

*Employee can work remotely anywhere in the U.S. The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of high quality documents and effective implementation of the writing process. Provides medical writing expertise for multiple c More...

*Employee can work remotely anywhere in the U.S. The Senior Medical Writer is responsible for providing medical writing ensuring successful preparation of high quality documents and effective implementation of the writing process. Provides medical writing expertise for multiple c More...

*Employee can work remotely anywhere in the U.S.  The Principal Medical Writer is responsible for providing writing support and advanced scientific writing expertise to the teams ensuring successful preparation of high quality documents and effective implementation of the wr More...

About This Role The Associate Director Quality Assurance & Governance R&D Quality & Compliance (RDQC) will provide strategic guidance oversight and support for the quality activities within the Quality Management System (QMS) including regulatory health inspections and th More...

What Does A Director Medical Writing DoThe role of a Director Medical Writing involves leading the creation of highquality medical content and ensuring compliance with regulatory standards. Here are some key responsibilities and qualifications for this position: Key Responsibilit More...

Position SummaryThe Indiana University Luddy School of Informatics Computing and Engineering IU Indianapolis campus invites applications for one open rank tenured or tenuretrack assistant associate or full professor positions in HumanComputer Interaction for the Department of HumanCe More...