Find Amazing Talent Find Your Dream Job

Clinical Research Associate

Contract: Alameda, California, US

Salary Range: 45.00 - 50.00 | Per Hour

Job Code: 362805

End Date: 2025-07-10

Days Left: 21 days, 14 hours left

To discuss more about this job opportunity, please reach out to Himanshu Kumar Singh(LinkedIn URL - https://www.linkedin.com/in/himanshu-kumar-singh-57b782258/), email your updated resume at Email - himanshu.ksingh@collabera.com or give me a call at (425) 403-0902. Thank you!
 
Pay Rate: $45- $50/hour
 
Position Details:
Industry: Pharmaceutical 
Job Title: Clinical Research Associate
Location: Alameda, CA 94502 (Hybrid)
Duration: 6 months (possible extensions)

Job Description:

  • This position will include monitoring and oversight of clinical sites to ensure timely and successful execution of clinical studies, resolving study-related discrepancies.
  • This position will ensure compliance with protocol and all regulatory policies, procedures, and/or guidelines during clinical studies by training/guidance of investigators/study coordinators, and follow-up of corrective actions.
  • Also, will ensure validity of study by identifying/resolving discrepancies and obtaining missing data and may track more routine aspects of a study. of clinical documents, which may include protocols, case report forms (CRFs), memos, correspondence, reports, and other required documents. Also, conduct new CRA orientation, onboarding, and training activities.
  • Candidate will proactively identify, and address issues related to study monitoring and clinical site management.
  • Track and communicate monitoring and site management updates and issues; escalate monitoring-related study timeline and quality risks to the Clinical leadership.
  • Maintain clinical operations processes, new employee onboarding, internal protocol training, monitoring tracking tools and study tools/templates for CRAs and site personnel.
  • Manage CROs/vendors for outsourced activities as applicable, including sponsor oversight of relevant functional activities (e.g., study management, monitoring, site management, project master files, and data management).
  • Ensure adherence to Good Clinical Practices, Industry standards, standard operating procedures and to all other regulatory and quality standards in conducting Lingo Clinical research and development.
  • Operate under minimal supervision and demonstrate a high degree of proficiency.
  • Undertake additional projects and tasks as determined by department and organizational needs.
  • The successful candidate will demonstrate the ability to work collaboratively across
    cross-functional teams, including Quality, Compliance, Product Development, and Engineering, etc.
  • They should have prior experience in Clinical Research or Clinical Trials and a solid understanding of related processes.
  • This role requires someone who is a quick thinker, adaptable to evolving workflows, and proactive in seeking clarification when needed.
  • This role requires a resourceful and agile individual who can think critically, adapt to evolving workflows, and proactively seek clarification when needed. The ideal candidate will also demonstrate creativity in problem-solving and be open to exploring innovative ideas and process improvements.
  • The ideal candidate must be able to quickly learn internal processes and demonstrate the ability to work independently with minimal supervision.
  • While support is always available, this role requires someone who can take initiative and adapt quickly in a fast-paced environment.
 
Education:
  • Bachelor’s degree-Major/Field of Study- Biology, Health Sciences, Mathematics, Computer Science, or equivalent
    Licenses and Certifications
Job Requirement
  • Clinical Research
Reach Out to a Recruiter
  • Recruiter
  • Email
  • Phone
  • Himanshu Singh
  • himanshu.ksingh@collabera.com
Apply Now
Apply Now
close-icon