Clinical Trial Associate I

South San Francisco, CA | Contract

Post Date: 07/27/2017 Job ID: 11653 Industry: Clinical & Scientific

Bayside Solutions is seeking a Clinical Trial Associate I to be part of our Client’ s team in South San Francisco. This is an opportunity to work with a local Biotechnical company focusing on the discovery, development, manufacturing and commercialization of medicines to treat patients with serious or life-threatening medical conditions.

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

Clinical Trial Associate I

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:
  • Develop, maintain and manage appropriate study documentation.
  • Collect, review and approve regulatory documents from clinical sites.
  • Initiate, maintain and reconcile Trial Master File.
  • Set up and maintain tracking systems and tools and report study metrics to support the clinical study.
  • Coordinate communication of tracking information within Study Team and to sites.
  • Manage and track clinical and non-clinical supplies.
  • Manage and track study-specific payments.
  • Coordinate investigator meeting planning in concert with travel planners, including preparing meeting materials and on-site meeting implementation (as requested).
  • Develop study related documents in collaboration with the study team.

Required Qualifications:
  • A Bachelor’ s degree in a medical/science related field is highly desired.
  • 2+ years’ experience demonstrating knowledge and understanding of clinical trials, such as that obtained in a clinical trial monitor capacity, and experience managing projects.
  • Demonstrated knowledge and understanding of ICH-GCP, the regulatory, ethics and contractual requirements for starting clinical trials.


Allison Glogovac

Making a positive impact is very important to me. Which is one of the main reasons why I love what I do at Bayside Solutions. I get the chance to support companies that are making a difference in the health, treatment, and wellness of patients across the globe. I strive to be a cut above my competitors by intently listening, learning about your career goals, and identifying the types of positions that you are excited about. If you have a passion for working within clinical research and are looking to explore amazing opportunities with companies where you can make a difference, let’s link up today. I look forward to meeting you!

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