JD for Clinical research coordinators
at Epsilon Clinical Research Pvt Ltd in Mangalore
- Published on 02-08-2011
- Viewed: 97 times
- 0 applicants
JD for Clinical research coordinators Qualification: MSC - Bio Science and life sciences) Experience: 0- 1 Year Location: Anywhere in South India Responsibilities: 1. Documentation 2. Collection of information of studies 3. Patients feedback collection etc Experience: 0 – 3 Years - Fresher’s can also apply Languages Known: English Hindi and Malayalam. Other Responsibilities Coordination and management responsibilities Serve as focal point for the clinical site for communication with MVI, GSK, and QUINTILES. 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 investigator’s 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. Organize and participate in the site initiation visit and accompany the monitor during monitoring activities. 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. Develop a tool for tracking home visits conducted by the clinical study fieldworkers. Ensure inventory of clinical supplies is completed. Play a role in developing and implementing a recruitment plan to ensure long-term recruitment target is met. Monitor enrollment and provide enrollment updates for the clinical team and the sponsors. Develop, in collaboration with the investigators and site staff, the site-specific protocol documents and the informed consent document, with assistance from the sponsors. Prepare appropriate individuals to disseminate information to health care professionals and the community to educate them regarding research activities. 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. Send your resumes/CV to hrd@epsilon.net.in with your detailed experience also you can contact us on my numbers+91 9980168506 or call +91 0824 2438700 ext number 26 . You can also walk in to out office address as mentioned below and drop in your resume personally. Epsilon Clinical Research Pvt Ltd 4th floor omega hospital near pumpwell circle kankanady bypass road mangalore 575 002 website: www.epsilon.net.in (M) +91 9980168506 (L) +91 0824 2438700 please connect to Ext no : 26