The right talent can transform your business—and we make that happen. At Collabera, we go beyond staffing to deliver strategic workforce solutions that drive growth, innovation, and agility. With deep industry expertise, a global talent network, and a people-first approach, we connect you with professionals who don’t just fit the role but elevate your business. Partner with us and build a workforce that powers success.
Clinical Data Coordinator
Contract: Abbott Park, Illinois, US
Salary Range: 35.00 - 40.00 | Per Hour
Job Code: 366050
End Date: 2025-12-24
Days Left: 11 days, 22 hours left
To Discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL - www.linkedin.com/in/deepak-arya-8a79aa22a/), email your updated resume at Email - deepak.arya@collabera.com. Thank you!
Pay rate: $35 - $40/hr. (Negotiable)
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)
Industry: Pharmaceutical
Duration: 12 months
Description:
- Oversee the production of Laboratory Systems Operations (LSO) deliverables for assigned clinical trials.
- Oversee all LSO timelines for assigned clinical trials and cross-functional meetings for assigned clinical trials.
- Coordinate discrepancy resolution efforts needed for complex issues that arise with the sample receiving team.
- Represent LSO team in vendor meetings to ensure timely response to projects and/or identified issues.
- Act as primary liaison with Regulated Bioanalysis, Biomarker Groups and Central Labs to ensure that priority project deliverables are met.
Major Responsibilities:
- Plans and manages LSO timelines for assigned clinical trials, specifically the completion of the Lab Specifications and Kit Delivery.
- Participates in vendor meetings to ensure proper representation for LSO and timely resolution of outstanding issues.
- Manages all process flows and data exchanges with any vendors or internal data providers/consumers.
- Assists with the development and review of trial-specific SOW, Laboratory manuals, Data mapping documents based on parameters supplied with MSA with applicable vendors and clinical protocol.
- Participates in cross-functional meetings where LSO tasks are discussed.
- Continually seeks to improve existing processes.
- Develops productive collaborations and communication with other cross functional groups.
- Ensures compliance with current SOPs. Participates in any internal quality assurance audits.
- Manages sample storage volumes and the sample lifecycle management process.
Qualifications:
- Bachelor’s degree in life sciences or equivalent field of study is required.
- Knowledgeable in clinical trials the end-to-end GLP, clinical study and sample lifecycle.
- 1-3 years of clinical study involvement and/or sample processing experience in a GLP regulated environment preferred
- Laboratory automation experience is a plus.
Job Requirement
- Clinical Trials
- Clinical Data
- Samples
- Vendor meetings
- SOP
Reach Out to a Recruiter
- Recruiter
- Phone
- Deepak Arya
- deepak.arya@collabera.com
Apply Now
Apply Now
