Clinical Research Coordinator I — Impactful Trials & Growth

Hassman Research Institute, LLC

Marlton (NJ)

On-site

USD 54,000 - 69,000

Full time

6 days ago
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Job summary

CenExel Clinical Research is seeking a Clinical Trial Coordinator in Marlton, NJ. The role supports coordinating trials in line with ICH and GCP guidelines, ensuring protocol adherence and data integrity. Strong communication and regulatory knowledge are essential.

The position offers full-time employment with competitive compensation and benefits after 30 days, including health, dental, vision, LTD, STD, life insurance, and 401k. Overnight travel may be required.

Qualifications

  • 0-3 years of experience in the medical field.
  • Knowledge of Federal regulations protecting human subjects in research.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

Responsibilities

  • Assists with coordinating all aspects of patient involvement from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assumes other duties and responsibilities as assigned.

Skills

Medical field experience
Regulatory knowledge
Leadership
Communication skills
Team collaboration
Crisis management
Independent worker
Data collection and reporting

Education

High school diploma
Bachelor’s degree preferred

Job description

CenExel Clinical Research is seeking a Clinical Trial Coordinator in Marlton, NJ. The role supports coordinating trials in line with ICH and GCP guidelines, ensuring protocol adherence and data integrity. Strong communication and regulatory knowledge are essential.

The position offers full-time employment with competitive compensation and benefits after 30 days, including health, dental, vision, LTD, STD, life insurance, and 401k. Overnight travel may be required.

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