Clinical Research Jobs in Kennewick, WA

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...

Job Quick Facts: Specialty: Rheumatology Job Type: Locum Tenens Facility Location: Kennewick WA Service Setting: Outpatient Reason For Coverage: Supplemental Coverage Period: Nov 3 2025 - Dec 31 2026 Coverage Type: Clinical Only Shift Schedule: 2 weeks on/2 we 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...

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...

STRATEGIC ACCOUNT MANAGEMENT & DEVELOPMENTDeep understanding of Vending & Transportation Sectors strategies drivers and approach to category and item management customer relationship building and selling. Collect and analyze relevant category customer and consumer data to info 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...

Tasked with implementing the vision and process framework of the CDMSO team by advising employees and teams on executing continuous improvement initiatives. This role coordinates highly effective teams by developing staff and delegating appropriate work assignments and priorities to e More...

AbbVie Data Science is the best-in-class team within its cross-industry peer group and isresponsible for bringing people process and technology together to generate business value fromclinical trials data. Our operational model is exemplified through execution and innovation. This rol More...

AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people process and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This r More...

The Senior Associate Trial Disclosure will be responsible for providing writing support to clinical trial registration and results postings including scientific study results and or protocol/results lay summaries and meeting required deadlines. Also responsible for the planning and ex More...

WHAT DOES AN ASSOCIATE DIRECTOR MEDICAL DOThe Associate Director Medical has a deep understanding of the clients business and demonstrates critical thinking and confidence while distilling the scientific and clinical data of the clients brand(s) their competitors and clinical landscap More...

In clinical research feasibility is often what determines whether a study succeeds or fails. Your insights will directly influence how trials are set up how quickly they recruit and how successful they are in meeting their goals. This is a high-impact strategic role for someone who en More...