Kelly Services
Location
Rye Brook, NY | United States
Job description
Clinical Research Data Coordinator
U.S. Based - Fully Remote- Part-Time: Short Term Contract 3-6 months with Potential to Extend
Kelly Science & Clinical®is currently hiring a Clinical Research Data Coordinator for one of our clients who is one of the leaders in the fight against blood cancer. We are seeking a motivated and detail-oriented Clinical Research Data Coordinator to join their dynamic team and contribute to groundbreaking research studies and trials. A Clinical Research Data Coordinator plays a critical role in the advancement of medical knowledge and the development of new treatments and therapies through tracking and cleaning the data obtained by study participants. This position requires attention to detail, a commitment to ethical research practices, and a strong ability to work in a collaborative, interdisciplinary environment.
General Responsibilities:
The Clinical Data Coordinator will be responsible for clinical data entry activities for the protocols and projects as directed. The position will ensure the highest standards for clinical data integrity and quality maintained in alignment with critical research efforts aimed to improve the treatment, health and medical outcomes of oncology patients.
Duties:
Responsible for the collection and review of clinical protocol research data; Interpretation of data including appropriate source documentation for entry into computerized databases
Good understanding of data definitions and case report forms and other information related to data collection for clinical research.
Must respond to queries in a timely fashion.
Main Responsibilities:
Responsible for the abstraction, entry, and general management of study data for clinical trials.
Assists with collection, entering, cleaning, maintenance and reporting of clinical research data
Enters protocol, medical history, and demographic information abstracted from patient charts into appropriate data capturing system EDC
Follow protocol design to assure all protocol data elements are collected in accordance with protocol guidelines
Update the EDC following verification of subject data, including the resolution of data queries Track site goals and case report form completion.
Maintain study specific documentation. Perform QC audits of the clinical database. Support and adhere to Good Clinical Practices GCP guidelines, FDA, Institutional Review Board IRB and HIPAA regulations, Site Operating Procedures and ethical standards for the conduct of research clinical trials.
Maintain to LLS and Site requirements for source document management and request for information. Communicate effectively with the Research Team, Investigators , Clinical Research Associates , Study Sponsor and ancillary staff.
Qualifications Required:
Position requires 3-5 years of experience in data collection activities within a GCP/clinical research regulatory environment.
Knowledgeable in critical elements for success in clinical trials, GCPs, ICH, and Code of Federal Regulations.
Clinical study experience in Oncology.
Strong medical terminology understanding.
Experience with EDC systems. Proficient in Microsoft Office Suite.
Pay $35/hour
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As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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