Clinical Trials Jobs in Gilbert, AZ

Job DescriptionThe Executive Medical Director is responsible for the safety strategy for solid tumors late-stage oncology portfolio and to supervise manage and mentor the safety physicians (Group MDs Senior MDs and medical directors) and supporting the Solid Tumor in the Oncology TA. More...

Whats In It for You:This is an exciting leadership opportunity for a person with passion and talent. The company believes that medical writing is a science that continuously evolves with new regulations and technologies.  The role provides the ability to influence company leaders More...

The Associate Director Statistics - Oncology provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials patient safety and global medical affairs (GMA). The Associate More...

Job Description: This role will provide support to key Global Site Contracting (GSC) Systems and technological solutions to manage the execution of clinical trials. The role successfully integrates GSC system capabilities to support effective system solutions. Requires frequent intera 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...

 *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...

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...

Roles & Responsibilities: MS in Statistics Computer Science or a related field with 5 years of relevant experience. or BS in Statistics Math Computer Science or a STEM related field with 8 years of relevant experience. SAS certification. Group setting SAS EG and Unix environment. SAS 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...

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...

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...

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...

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...

Job TItle: Global Medical Affairs Liver Diseases / Virology Job Duration: 6 months Job Location: Foster City California Job Description Reporting to the Sr. Director of Viral Hepatitis Global Medical Affairs this role is a key position within the Global Liver Inflammation Virol More...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. Th More...

Job Title : CMC Technical Writer Job Location: Santa Monica California Job Duration: 6 months; May extend highly motivated individual with late-phase CMC technical experience including technical and regulatory submission experience. This position is part of the Process Developmen 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...

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...

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...