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Clinical Research Coordinator - Dana-Farber Cancer Institute at South Shore Hospital

South Shore Health System

Weymouth

On-site

GBP 60,000 - 80,000

Full time

30+ days ago

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Job summary

An established industry player is seeking a Clinical Research Coordinator to support its Clinical Trials Research Program. This role involves registering patients, maintaining trial databases, and assisting with data collection for clinical trials. The ideal candidate will possess strong communication skills and critical thinking abilities, working effectively within an interdisciplinary team. Embrace the opportunity to contribute to innovative research and enhance your skills in a supportive environment that values continued learning and technology adoption. If you are passionate about clinical research and eager to make a difference, this position is perfect for you.

Qualifications

  • Ability to work effectively in an interdisciplinary team.
  • Demonstrated skills in critical thinking and problem solving.

Responsibilities

  • Register patients to protocols and maintain trial databases.
  • Conduct phone interviews with potential trial participants.
  • Assist with data collection and prepare paperwork for new patients.

Skills

Critical Thinking
Problem Solving
Data Management
Communication Skills

Education

Bachelor's Degree in a related field

Tools

Database Management Systems
Data Collection Software

Job description

Job Description Summary

The Clinical Research Coordinator is responsible for administrative and data collection support of the Clinical Trials Research Program.

Job Description

ESSENTIAL FUNCTIONS

Essential functions are those tasks, duties and responsibilities that comprise the means of accomplishing the job's purpose and objectives. Essential functions are critical or fundamental to the performance of the job. They are the major functions that the person in the job is held accountable for. Following are the essential functions of the job:

  1. In collaboration with the Research Nurse, registers patients to protocols.
  2. Maintains trial database, including collecting and entering data.
  3. Completes all forms pertaining to protocols, and reporting of questions, discrepancies, and violations to protocol investigator and collaborating institutions and companies.
  4. Organizes monitoring visits.
  5. Copy, mail and/or fax all protocol patient records to the proper institutions.
  6. Assist with data collection for clinical trials as needed and submit to data management offices.
  7. Prepare paperwork for all new protocol patients.
  8. Conduct phone interviews with possible participants for trials.
  9. May handle specimens, including collection, appropriate packing and shipping of specimens in accordance with all safety regulations.
  10. Prepare/schedule patients for entry eligibility visit for potential study participants.
  11. Collects medical data from paper and electronic sources, both internal and external.
  12. Keep all consents and related forms/paperwork in a file system for easy reference with adequate copies available.
  13. Participates in internal and external audits.
  14. Assist the Research Nurse with any and all other necessary tasks. This includes phone calls, mailings, filing, and miscellaneous data management tasks.

Technology and Learning

a. Participates in continued learning and possesses a willingness and ability to learn and utilize new technology and procedures that continue to develop in their role and throughout the organization.

b. Embraces technological advances that allow us to communicate information effectively and efficiently based on role.

Demonstrated ability to work as an effective member of an interdisciplinary team. Demonstrated skills in critical thinking, problem solving, and ability to make independent decisions. The ability to balance multiple tasks and normal stress associated with the duties and responsibilities of this position are essential requirements in the performance of this job. The ability to speak, read, and write in English.

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