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Jefferson Health·Montgomery County, PA

Clinical Research Coordinator (Full time) Jefferson Moss-Magee Research Institute EP

Healthcare AdministrationFull time
✓Requirements
Certifications
✓Patient transporters can walk 8-10 miles per shift. *Patient care providers may be required to perform activities specific to their role including kneeling, bending, squatting and performing CPR.
Education
✓High School Diploma/GED or equivalent.
Qualifications
✓4 years of relevant experience.
✓Knowledge of and the ability to utilize technology tools to organize, store and manage database systems.
✓Knowledge of and ability to utilize tools, techniques and processes for gathering and reporting data in a particular department or division of a company.
✓Knowledge and understanding of legislation and regulatory bodies affecting healthcare practices
✓Knowledge of principles and practices associated with the rights and responsibilities of patients and caregivers.
✓Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation.
+Benefits
✓Medical, dental and vision
✓Tuition assistance
✓Retirement plan
✓Life and disability insurance
Pay for this position
Pay not listed
Apply to Jefferson Health ↗
Questions about pay or the unit? Ask a Waypoint recruiter.
✓You’ll need
Certifications
✓Patient transporters can walk 8-10 miles per shift. *Patient care providers may be required to perform activities specific to their role including kneeling, bending, squatting and performing CPR.
Education
✓High School Diploma/GED or equivalent.
Qualifications
✓4 years of relevant experience.
✓Knowledge of and the ability to utilize technology tools to organize, store and manage database systems.
✓Knowledge of and ability to utilize tools, techniques and processes for gathering and reporting data in a particular department or division of a company.
✓Knowledge and understanding of legislation and regulatory bodies affecting healthcare practices
✓Knowledge of principles and practices associated with the rights and responsibilities of patients and caregivers.
✓Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation.
+Benefits
Medical, dental and visionTuition assistanceRetirement planLife and disability insurance

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About the role

Works under limited supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database management, biological specimen processing, and clerical duties) to assist investigators in organizing, gathering and compiling clinical research data.