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Fortis Healthcare Limited is committed to clinical excellence and patient-centric healthcare, which is manifest in hospital design, patient services, medical programmes and the compassionate approach of medical and non-medical hospital staff. Fortis commissioned its first hospital in 2001 at Mohali, near Chandigarh, and has expanded its operations to become a network with an over 10,000 bed capacity across 68 hospitals.
Job Title : Clinical Research Co-ordinator
Desired Profile : Preferably MSc Clinical Research with 2 to 5 years experience
Experience : 2 – 5 Years
Location : Bengaluru/Bangalore
Openings : 1
Job Description
- Interviewing and enrolling eligible participants into the study.
- Responsible for ensuring that any study under his/her supervision is in compliance with good clinical practice guidelines.
- Ensure that forms detailing a study are correctly filled out and are properly filed.
- Compilation, collection and documentation of research data.
- Responsible for enrolling patients and assuring compliance for all patients.
- Play an integral role in managing the overall site staff, this involves human resource and logistical issues.
- Oversee overall clinical operations related to conduct of the trial (i.e. recruitment, informed consent procedure, visit coordination, sampling, visit scheduling, etc).
- Work in collaboration with study team to ensure trial preparedness.
- Attend and participate in investigators meetings, stakeholders meetings, and other meetings as needed.
- Serve as point person at the clinical site for monitoring needs.
- Prepare monitoring visits to make sure monitors receive all necessary information during their visits.
- Review protocol with the clinical team and ensure clinical team is aware of their roles and responsibilities.
- Develop reporting mechanism for bringing critical and high priority issues to the investigators, study sponsors, and/or the monitors.
- Develop an internal system for quality assurance.
- Play a role in developing and implementing a patient recruitment plan to ensure long-term recruitment target is met.
- Develop or improve system of maintaining subject files.
- Ensure timely and accurate transcription of information on source documents, paper case report forms (CRFs), and electronic CRFs.
- Schedule trainings as needed for the site staff.
- Participate in data query resolution process
