Clinical Research Coordinator - Jefferson University
Overview
Lead day-to-day clinical trial operations ensuring GCP compliance while supporting investigators with database management and specimen processing. Manage documentation and communicate patient outcomes to the Principal Investigator. Optimize data workflows using Python and AWS. Drive efficient processes that streamline research activities across teams.
What You'll Do11
- 1Interact with co-workers and visitors consistent with Jefferson values
- 2Perform research database tasks and biospecimen collection
- 3Maintain required clinical trial documentation
- 4Inform PI about patient responses and adverse effects
- 5Assist with regulatory filings such as IRB submissions
- 6Support subject enrollment and clerical/technical needs
- 7Ensure protocol adherence and data quality
- 8Manage multiple priorities and time effectively
- 9Lift and carry patient loads up to 50 lbs
- 10Stand/walk continuously with occasional strenuous activity
- 11Provide CPR if required by role
Requirements10
- 15+ years building ETL pipelines with Spark and Airflow
- 24 years of relevant experience
- 3Knowledge of data organization tools and techniques
- 4Understanding of healthcare legislation and regulatory bodies
- 5Ability to prioritize and allocate time effectively
- 6Physical capacity to lift 40-50 lbs
- 7Experience with patient transport and mobility demands
- 8Education with high school diploma or equivalent
- 9Familiarity with patient rights and caregiver responsibilities
- 10Commitment to managing concurrent objectives
Salary Insight
Salary not disclosed in listing
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
Thomas Jefferson University and Hospitals
VerifiedResearch Tech, Clinical Research & Data Management
You will own the data flow and sample processing for clinical research studies at Jefferson, supporting over 65,000 patients and 32 hospitals. You will work with RedCap, Python, and SQL in a team of researchers and clinicians. This role delivers clean, organized data for translational research and clinical trials.
Thomas Jefferson University and Hospitals
VerifiedClinical Research Assistant Oral Maxillofacial Surgery
Jefferson seeks a Clinical Research Assistant to support the Oral & Maxillofacial Surgery department. The role involves organizing and compiling clinical research data while tracking credentialing documentation for staff and researchers. Candidates will provide clerical and technical support to ensure protocol adherence and quality of information.
Insight Global
VerifiedClinical Research Coordinator Insight Global
We seek a dedicated Clinical Research Coordinator to lead oncology trials in Philadelphia offering hybrid flexibility. This full-time day shift role requires a bachelor's degree and three years of experience. Join our dynamic team to advance medical knowledge through rigorous research practices.
Actalent
VerifiedSr Clinical Research Coordinator Oncology
Lead senior clinical research coordinator overseeing study execution for diverse portfolio of investigator initiated and industry sponsored trials. Seeking proactive research professional passionate about clinical research patient care and driving innovative therapies.
DocTrials
VerifiedClinical Research Coordinator - DocTrials
Coordinate patient visits and lead interventional protocols at multiple Phoenix Valley offices. Manage patient acquisition and enrollment through community outreach while ensuring strict adherence to FDA and ICH-GCP guidelines. Consolidate study data and communicate updates via Basecamp.
Vanderbilt Health
VerifiedClinical Research Coordinator I Vanderbilt Health
Responsible for coordinating approval processes and conduct of research protocols while maintaining integrity and quality of clinical research. Prepare and process new IRB research proposals amendments continuing review applications and adverse event reports. Maintain documents required for internal regulatory and sponsor access. Perform site visits to review research and source documentation. Procure equipment and supplies. Record data onto case report forms. Attend queries promptly. Ensure compliance with regulations and good clinical practice. Package and ship specimens following guidelines. Assist with study completion closeout and archiving. Develop and manage study budgets. Advocate for human subjects through communication with investigators and participants. Determine eligible candidates assessing medical history. Communicate positively with participants and coworkers. Perform or instruct others in protocol procedures. Report deviations to PI. Provide support to research faculty and staff.