ConcertAI job vacancy for Clinical Research Data Coordinator | Apply Now
Clinical Research Data Coordinator
Location: Bengaluru, Karnataka, India
ConcertAI is a fast-growing healthcare research organization, leading the market in oncology healthcare data analytics. We are assembling a talented team to join us on our mission to transform how clinical insights are generated and to accelerate therapeutic innovations to patients. Our dynamic, fun, and highly experienced team is looking for a Clinical Reseach Data Coordinator to join our expanding team.
Work Experience
Responsibilities :
-Review project specific documents, as needed, to develop familiarity with project goals and with the data abstraction tasks in each
– Perform prescreening activities using the DTS eScreening tool to determine likely eligibility for a clinical trial.
– Undertake medical record reviews to populate and annotate EMR data for eCRF entry.
– Support site use of the DTS and DTS system interactions with target EDC systems.
– Detect issues related to data capture, collection or management and suggest solutions.
– Assist in investigating incomplete, inaccurate, or missing data and documents to ensure accuracy and completeness of data ingestion for AI Machine Learning and AI Modeling.
– Provide subject matter expertise on clinical trial data entry into EDC systems utilized by sites and for leveraging on internal projects.
– May work with partner vendors, internal product and engineering teams, as well as IT and clinical research informatics staff to suggest improvements in hardware and software functionality for Clinical Data Coordinator and Site Staff workflows.
– Interact internally with the other Data Coordinators, Clinical Project Managers, Director of Clinical Delivery and other DTS staff regarding ongoing and planned projects.
– Be responsible for organizing study related material and attend study relevant meetings with clinical research site staff and support with use of DTS modules.
– Respond promptly to questions from the larger DTS team or other project personnel.
– Attend departmental and project-specific meetings as scheduled.
– Participate in training sessions for each assigned project, as applicable.
Requirements
Associate degree or equivalent from two-year college or technical school; OR one to two years related experience and/or training; OR equivalent combination of training and clinical experience.
Clinical site and clinical research experience is required.
Bachelor’s degree or RN license strongly preferred, or international equivalent.
Experience in the field of Oncology is highly
Experience with medical records, clinical trial data entry into eCRFs, chart audit, or coding is
Experience recruiting, screening, and enrolling study participants who meet research criteria as well as obtaining informed consent and collecting and entering subject trial data consistent with research protocols is strongly
Experience managing and submitting study protocols, amendments, consent forms, and patient recruitment materials to the Institutional Review Board is desirable.
Must be organized, detail-oriented, and able to coordinate multiple projects with shifting priorities
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Must be able to work independently and as a part of a team
Demonstrates the tenacity to learn and adapt quickly
Has a strong work ethic and is comfortable under the pressure of tight deadlines
Strong proficiency in the entire Microsoft Office Suite
High comfort-level with new technologies, collaboration tools for communication and document sharing
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