Full-time
Clinical Research Coordinator, RN
Competitive
Grand Rapids, MIScience & PharmaceuticalPosted 18d ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
18 days ago
Job description
Responsibilities
Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study
Create/review forms created or revised for assigned trials to assure protocol compliance
Maintain files using standardized study document labeling and filing procedures
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management
Maintain an up-to-date contact list
Assist with patient screening and determination of eligibility
Facilitate the informed consent process ensuring that consent is appropriately completed
Prepare and manage source documents according to standard operating procedures
Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations
Assist data coordinator team with case report form completion and query resolution
Work with the Principal Investigator to complete and submit Serious Adverse Event reports
Perform protocol specific closeout related activities in conjunction with the data coordinator
Provide documentation for all deviations whether related to the protocol or a SOP
Ensure that all team members involved understand and adhere to assigned protocols
Perform telephone triage assessments of patients on trial when necessary
Provide patient education regarding participation in a clinical trial, chemotherapy/biotherapy/investigational agent administration and potential side effects
Preferred
Bachelor's degree in Nursing
Experience working in an oncology setting
Benefits
Medical, dental, and vision insurance provided
401(k) plan available with employer matching
Life and disability insurance for added protection
Health savings and flexible spending accounts offered
Paid time off
Flexible schedule
Remote work choices
A collaborative, creative environment where employees can learn and grow and are encouraged to contribute to processes, decisions, planning, and culture
The START Center for Cancer Research is a oncology and biotechnology research company.
San Antonio, Texas, USA
https://startresearch.com
Late Stage
Total Funding
unknown
2024-04-03
Acquired
Leadership Team
Chris Takimoto
Global Chief Medical Officer
Recent News
PR Newswire
Allegheny Health Network and The START Center for Cancer Research Announce Strategic Collaboration to Expand Patient Access to Early-Phase Cancer Trials
2026-08-25
Bizjournals.com Feed (2025-11-12 15:43:17)
AHN teams up with START Center to expand early-phase oncology research in western Pennsylvania
Baptist Health South Florida and The START Center for Cancer Research Announce Strategic Partnership to Expand Patient Access to Early-Phase Cancer Trials
2026-05-28
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Qualifications
Associate's degree in Nursing
RN license in state practicing
2 years of clinical research experience
Basic understanding of oncology clinical trials, particularly Phase 1 studies
Strong attention to detail and accuracy in data collection and documentation
Ability to manage multiple tasks and meet deadlines in a fast-paced environment
Excellent organizational and time-management skills
Strong communication skills, both written and verbal
Ability to interact professionally with patients, study staff, and external stakeholders
Working knowledge of GCP and regulatory requirements
Proficient in Microsoft Office Suite and clinical trial management software
Bachelor's degree in Nursing
Experience working in an oncology setting
2 years of clinical research experience.
Required skills
Registered Nurse (RN) License, Oncology Clinical Trials, Phase 1 Clinical Trials, Clinical Practice (GCP), Clinical Trial Regulatory Requirements, Microsoft Office Suite, Clinical Trial Management Software, Oncology
Preferred skills
Bachelor's degree in Nursing, Experience working in an oncology setting
Experience
2+ years
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