Fortis Healthcare Limited is a leading integrated healthcare delivery service provider in India. The healthcare verticals of the company primarily comprise hospitals, diagnostics and day care specialty facilities. Currently, the company operates its healthcare delivery services in India, Dubai, Mauritius and Sri Lanka with 45 healthcare facilities (including projects under development), approximately 10,000 potential beds and over 374 diagnostic centres. For more information, please visit
Date and Time:
30 September – 1st October , 9.30 AM – 5.30 PM
Fortis Hospital, Bannerghatta Road Bangalore
Contact – Prathap N ( 8310558330 )
1 – 3 years
3-4 Lacs P.A.
Bengaluru( Bannerghatta Road )
Job description
Role & responsibilities:
- 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
Preferred candidate profile : 1-2 years of clinical research experience in hospital settings, complemented by an MSc in Biotechnology and a background in Pharmacy (B Pharma, M Pharma).
Perks and benefits: EPF, Health Insurance, Term Insurance, Personnel accodent insurance, discounted food, Free coffee/TeaRole:
Clinical research ScientistIndustry Type:
Medical Services / HospitalDepartment:
Research & DevelopmentEmployment Type:
Full Time, PermanentRole Category:
Pharmaceutical & Biotechnology
Education:
MS/M.Sc(Science) in Biotechnology, Bio-Chemistry, Microbiology
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