NEW JOB OPENING
CLINICAL RESEARCH SPECIALIST - CLINICAL TRIALS, RESEARCH COORDINATOR
IN Pleasanton, CA, USA!

 

Date Posted: 08/25/2026
Hiring Organization: Rose International
Position Number: 506295
Industry: Healthcare
Job Title: Clinical Research Specialist - Clinical Trials, Research Coordinator
Job Location: Pleasanton, CA, USA, 94588
Work Model: Hybrid
Work Model Details: 2 days a week (Tues, Wed) onsite
Shift: 8 AM to 5 PM
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 4
Min Hourly Rate($): 27.00
Max Hourly Rate($): 30.00
Must Have Skills/Attributes: Healthcare, Rave, Tracking
Experience Desired: Study tracking data base and the clinical trials platforms, (3 yrs)
Required Minimum Education: High School Diploma or equivalent

**C2C is not available**

 

Job Description


• Required Education: High School Diploma





Description of Project:

• This study, the Five or Ten Year Colonoscopy for 1-2 Non-Advanced Adenomatous Polyps (FORTE), aims to determine the benefit, optimal timing and recommended frequency of surveillance colonoscopies after a colonoscopy detecting 1-2 non-advanced adenomas

• This is a clinical trial funded by NCI.

• As the practice of colonoscopy expands to include the vast majority of adults and the detection of adenomas at colonoscopy increases, the inconvenience, medical risk, and resources associated with and devoted to surveillance colonoscopy will greatly increase

• Research to determine the benefit and yield of surveillance colonoscopy in patients with non-advanced adenomas is a high priority because of the high prevalence of adenomas

• The results of this study will impact decisions regarding repeated performance of colonoscopy procedures, which affect large portions of the population over age 50.



We are seeking a Rsch Specialist II to support the following tasks:

• Conduct cohort ascertainment through the review of colonoscopy and pathology reports; determine study eligibility;

• Assemble and mail weekly (stool/blood) and annual mailings;

• Conduct reminder calls to participants to complete survey, stool kits, and other data collection; respond to participant inquiries via email and phone;

• Data enter questionnaires and other data collection points into study tracking data base and the clinical trials platforms, iMedidata (RAVE) and OPEN;

• Assist with initial enrollment, upload reports to reporting platforms, data enter required information;

• Follow all project recruitment protocols.
  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**


 

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).

 

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About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.

David, Consultant

I am very happy with the Rose International, and the professionalism of the employees.

Robin, Consultant

Working for Rose International was the most pleasant assignment I have ever had. They were always on top of situations when necessary, and very helpful. I was very proud to be an employee of Rose International, and would recommend anyone to try to work with them.

Melvon, Consultant

My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.

Diana, Consultant

Rose International maintained good communication during assignments and are very informative through email and phone calls.

Sade, Consultant

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