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Clinical Research Coordinator - SKCC

Davita Inc.

Philadelphia (Philadelphia County)

On-site

USD 50,000 - 70,000

Full time

3 days ago
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Job summary

A leading healthcare organization in Philadelphia is searching for a Clinical Research Coordinator. This role focuses on managing clinical trial activities, including data management and ensuring compliance with regulatory standards. Candidates must possess a High School Diploma, relevant experience, and strong organizational skills.

Qualifications

  • Minimum High School Diploma required.
  • 4 years of relevant experience preferred or higher education degree with prior experience.
  • Must assist in regulatory filings and patient interactions.

Responsibilities

  • Oversee the day-to-day activities of clinical trials.
  • Perform database management and biological specimen processing.
  • Recruit and assist with consenting subjects.

Skills

Research
Database Management
Clerical Duties

Education

High School Diploma or equivalent
Bachelor's or Master's degree

Job description

Job Details

Clinical Research Coordinator - SKCC

Job Description

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. Recruits, assists with consenting subjects, and conducts study visits.

Essential Functions:

  • Interacts with co-workers, visitors, and other staff consistent with the values of Jefferson.
  • Performs research, database, biospecimen collection and processing, as well as clerical duties to support clinical trials and assist investigators.
  • Organizes and maintains documentation required for clinical trials.
  • Informs Principal Investigator and/or designated individuals of any issues concerning patient responses to treatment, medication, or adverse effects.
  • Assists with regulatory filings, including IRB submissions.
  • May assist in enrolling human subjects and provide clerical and technical support to ensure protocol adherence and data quality.

Minimum Education and Experience Requirements:

  • Education: Minimum High School Diploma or equivalent.
  • Experience: High School Diploma or equivalent with 4 years of relevant experience, or a Bachelor's/Master's degree with preferred prior experience.

Work Shift: Rotating (United States of America)

Worker Sub Type: Regular

Primary Location Address: 1101 Market, Philadelphia, Pennsylvania, United States of America

Jefferson, located in the greater Philadelphia region, Lehigh Valley, Northeastern Pennsylvania, and southern New Jersey, is reimagining health care and higher education to create value. With over 65,000 staff, Jefferson provides high-quality clinical care, advances research, and educates future professionals across its colleges and schools.

Jefferson is committed to equal opportunity employment for all persons regardless of age, race, color, religion, creed, sexual orientation, gender identity, marital status, pregnancy, national origin, military or veteran status, disability, or any other protected status.

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