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Client Study Coordinator
Client Study CoordinatorVarite • West Sacramento, CA, United States
Client Study Coordinator

Client Study Coordinator

Varite • West Sacramento, CA, United States
[job_card.1_day_ago]
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  • [job_card.full_time]
[job_card.job_description]

VARITE is looking for a qualified Client Services Study Coordinator in West Sacramento, CA.

WHAT THE CLIENT DOES?

An American-headquartered life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.

WHAT WE DO?

Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services.

Job Title : Client Services Study Coordinator

Location : West Sacramento, CA

Contract Duration : 12 months

Pay Rate Range : $25.00 - $27.50 / hr on W2

HERE'S WHAT YOU'LL DO :

Responsibilities :

  • Point person for the facilitation of Clinical Trial Testing; bridges the sponsor and trial execution by managing client relationships and overseeing trial progress.
  • Manage all aspects of assigned trials under your purview with direction from the lead Project Manager.
  • Communicate with clinical and regulatory affairs and translate information effectively. This includes all matters; technical, facilitation of workflow, testing sites and customer relations.
  • Maintain up to date and accurate logs reflecting testing status.
  • Provide metrics to the site, customer or sponsor as requested.
  • Resolve issues as they arise. Report critical issues to site leadership.
  • Provide updates as requested.
  • Develop SOPs supporting clinical trial testing as required.
  • Maintain Study Binders / Trial Master File (TMF) as required per GCP.
  • Perform Quality checks on all deliverables to customers. Partner with other employees to ensure second QC checks when required.
  • Training other personnel as required.

Qualifications and Experiences :

  • Associate or bachelor's degree (AA or BS).
  • Two years' experience and / or training in related field such as in a Contract Research Organization, University or Medical setting, or other equivalent experience.
  • Experience working in regulated environments and familiarity with CAP / CLIA / CDx regulatory compliance and quality assurance standards.
  • Minimum of 2 years Study Coordinator or Clinical Research or Trial experience required.
  • Skills :

  • Demonstrated proficiency in computer skills, such as word processing, Excel and information systems.
  • Excellent verbal and written communication skills, customer service and problem-solving skills.
  • Strong attention to detail and understanding of regulatory compliance, GCP and HIPAA.
  • Knowledge of medical terminology.
  • Positive attitude and the ability to adapt and be flexible in a fast-paced and evolving work environment.
  • Organizational skillset, process driven, and able to manage multiple tasks with flexibility and ease.
  • If this opportunity interests you, please respond by clicking on EasyApply.

    Know someone who would be perfect for this role? Refer them to us and if they are hired, you could be eligible for our employee referral bonus! Help us grow our team with top talent from your network.

    VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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