Clinical Development Jobs in Canby, OR

 *This role could be based in lake county/ San Francisco or could be remote.Purpose:To lead Product Safety Teams (PST) and support one or more products as the PST lead alone or with other PST leads ensuring that the safety profile of one or more products is adequately monito More...

About The Position The KIPP Foundation is seeking a Director of Transformation to drive strategic change and innovation across its operations. The Senior Director will be responsible for leading strategic transformation efforts across KIPP Foundation teams (i.e. Finance Schools T More...

AECOM is seeking a Senior CEQA/NEPA Manager for one of our offices in Sacramento CA. This job is open to remote work.JOB SUMMARYThis role provides critical oversight and coordination of environmental processes to ensure timely delivery of project clearances. This role supports the dev More...

Provide strategic and operational support to the Area Head Clinical Site Management (CSM) in developing aligning resourcing and executing functional operational and financial priorities ensuring alignment with overarching Clinical Development Operations Clinical Site Management and ke More...

The Senior Director Clinical Value and Access Screening is a subject matter expert and key senior team member who embraces the challenge to lead an innovative approach to cancer screening.The Senior Director Clinical Value and Access Screening is a medical affairs professional who can More...

The Scientific Director Medical Affairs provides medical and scientific strategic and operational input into core hematology medical affairs activities such as: health-care professional and provider interactions (Payers Patients Prescribers and Providers); generation of clinical and s More...

Under the general direction of the Vice President manages the day-to-day operations and staff responsible for  both external and internal engagement on all California state regulatory matters.  For external engagement manages the ISOs participation in processes at the Califo More...

PurposeThe Medical Science Liaison (MSL) is a field based scientific expert that strategically supports the research and business objectives of a designated therapeutic area across the product life cycle. MSLs are the primary communicators of AbbVie science within a specific geography More...

THE POSITION:The Patient Service Coordinator is responsible for coordinating the onboarding of new patients. They fully populate the patients profile and enter their prescription details. The Sr. Patient Service Coordinator is a resource for the physician and their staff while initiat More...

Leads the development & execution of integrated value and evidence strategy for Obesity disease area and for ABBV-295.  Value and Evidence lead for Obesity engaging with cross functional teams and in the pipeline commercialization teams. Accountable for value and evidence str More...

Senior Regulatory Affairs Manager OncologyPosition SummaryThe Senior Regulatory Affairs Manager - Oncology will provide direct regulatory support for Oncology IVD/CDx products (Guardant360 CDx and future products such as Tissue IVD/CDx) in all stages of the product lifecycle. Th More...

The Senior Regulatory Affairs Manager - Screening will provide direct regulatory support for IVD cancer screening products (Shield CRC and future blood-based cancer screening tests) in all stages of the product lifecycle. This role will actively lead and support development and implem More...

The primary role of the Medical Affairs Director is to educate and develop clinical champions with the most current study findings supporting the clinical value of Guardant Healths product(s). The Medical Affairs Director will work in collaboration with the VP Medical Affairs Screenin More...

The Clinical Operations Program Director is responsible to connect science and operations to bring clinical studies to life through the execution of one or more clinical research programs .The Clinical Operations Program Director serves as a strategic advocate for pipeline assets and More...

Senior Regulatory Affairs Manager OncologyPosition SummaryThe Senior Regulatory Affairs Manager will provide direct regulatory support for Oncology IVD/CDx products (Guardant360 CDx and future products such as Tissue IVD/CDx) in all stages of the product lifecycle. This role will act More...

*Remote or Hybrid in AbbVie Location. Position title and grade level will be based on qualifications listed below and location hired.PurposeRole is responsible for leading evidence modelling teams to design and execute evidence-synthesis health economic models. Position applies method More...

Purpose:Group Medical Director manages other Associate Medical Directors Medical Directors Senior Medical Directors. Leading Product Safety Teams (PST) and PST leads (and could support one large product as the PST Lead) and ensuring safety of late stage and post marketing hematology-o More...

Eurofins Medical Device Consulting is seeking an experienced and influential Regulatory Affairs Thought Leader to serve as a strategic partner to our marketing and sales teams and a visible representative of our brand in the marketplace. This individual will elevate our presence at tr More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Home-Based in United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards re More...

The Director Clinical Operations will ensure that clinical stage programs achieve program objectives within established timelines budget and quality standards. This role involves contributing to the development of clinical program strategy providing leadership to the clinical operatio More...