Clinical Research Associate III

Emeryville, CA | Contract

Post Date: 08/28/2017 Job ID: 11846 Industry: Clinical & Scientific

Bayside Solutions is seeking a Clinical Research Associate III to be part of our Client’ s team in Emeryville. This is an opportunity to work with a Global healthcare company focusing on improving the health and well-being of people around the world. 

Our client is a Global sponsor company that develops innovative diagnostic therapies designed for hospitals, laboratory professionals and healthcare providers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Clinical Research Associate III

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs & study protocols. 
  • Ensures coordination of an accelerated study start-up including pre-study visits, initiation, interim, and closeout activities associated with clinical trials to ensure timelines & metrics are met & maintained throughout the study.

Required Qualifications:
  • Bachelor’ s degree in a life science field is required.
  • Typically requires 5 years of experience in clinical research, including a minimum of 2 years field monitoring experience and 3 years in lead CRA role.
  • Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, & company SOPs.
  • Excellent knowledge of therapeutic area assigned.
  • Excellent knowledge of ICH/GCP Guidelines & EDC process.
  • Strong verbal & written communication skills.
  • Ability to train others in using MS Office Suite & EDC systems.
  • Ability to meet deadlines, multitasks & prioritize based on study needs.
  • Ability to make sound decisions based on available information.
  • Ability to establish rapport with site personnel/ colleagues. 
  • Ability to work both in a team & independently.
  • Ability to facilitate team meetings & teleconferences. 
  • Ability to present at internal study team meeting(s).
  • Ability to train & mentor junior CRAs.
  • Ability to seek new learning opportunities within & outside of the assigned project.
  • Ability & willingness to travel.

 

Cori Cook

I have always been a people person. As a clinical recruiter at Bayside Solutions, I get to build lasting relationships with candidates and assist them in finding job opportunities that they are as passionate about as I am about recruiting. At Bayside we believe in providing our candidates with the best possible experience, by listening to what they want in their careers and pairing them with great companies. If you’re interested in new opportunities now or would like to connect for the future, I’d love to hear from you!

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