Crystal Equation
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Pay range is $87 - $104 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.
Clinical Trial Support Resource II
Description:
This position comes with full benefits, including medical, dental, vision, life, 401k and more!
THE PROMISES WE MAKE:
At Crystal Equation, we empower people and advance technology initiatives by building trust. Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start. We will serve to empower you along the way and provide the path for your professional journey.
Clinical Trial Support Resource II
1 Astellas Way Northbrook, IL 60062 US
Posted: 02/13/2023
2023-02-13
2023-04-27
Job Number: 36958
Job Description
Pay range is $87 - $104 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.
Clinical Trial Support Resource II
Description:
- Assist in the day to day support of study operations including tracking and creating overviews of subject, site, study status, milestones and performing quality check activities across components of the clinical study.
- Assist in study set-up including but not limited to eCRF design, protol preparation, informed consents, investigator selection, systems (e.g., CTMS, IVR, etc.), study related operational manuals, trainng materials, and various study plans (e.g., visit logs, drug inventory, monitoring plan, etc.)
- Process and track clinical trial materials requests, study related supply requests, safety letters, vendor and investigator payments and other study related activities as needed
- Assist in the management of study completion activities including data review and clinical study report review
- Ensure complete and timely collection and archiving of TMF documents of assigned studies or program, including oversight and/or submission of regulatory documents to the TMF and ongoing document reconciliation.
- Assist in maintaining accurate and up to date study information within CTMS and other relevant tracking systems
- Effectively communicate with study team members and work closely with Lead Study Manager to address challenges
- May participate in process improvement and quality-related initiatives associated with study execution and deliverables;
- Other duties as assigned
This position comes with full benefits, including medical, dental, vision, life, 401k and more!
THE PROMISES WE MAKE:
At Crystal Equation, we empower people and advance technology initiatives by building trust. Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start. We will serve to empower you along the way and provide the path for your professional journey.