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Bioinformatics Summer Internship 2024 With Hands-On-Training + Project / Dissertation - 30 Days, 3 Months & 6 Months Duration

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

Click to Apply Online

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