Position— Clinical Research Coordinator
Company– CYTENET
No of Opening- 03
Location– Pune, Ahmedabad, Mumbai.
Key Responsibility-
1 Coordinate & Oversee the day to day operation of clinical trails.
2 Assist PI in recruiting screening & enrolling study participants.
3 Assist PI in obtaining informed consent from study participants.
4 Schedule & Conduct.
5 Collect & Record accurate data in accordance with the study protocol.
6 Ensure compliance With the study protocol Good clinical practice (GCP)guidance & regulatory requirement.
7 Maintain study documentation & ensure data integrity.
8 Assist in preparing EC dossier for EC Submission.
9 Communicate effectively with study CRO, Sponsors. Investigator, EC & other stakeholder.
10 Monitor study progress & report any issues or deviations from the protocol to the study. sponsor or principal investigator.
11 Participate in site visits audit, & inspections as required.
12 Provide regular updates & reports to the clinical research team & management.
Qualification-
Master/ Bachelor degree in life sciences health care or a related field.
Previous experience in clinical research or a related fields preferred.
Knowledge of GCP, ICH guidelines & regulatory requirement.
Strong Organizational & time management Skills.
Excellent communication & interpersonal skill.
Attention to details & ability to maintain accurate records.
Proficiency in MS office & clinical trails management software.
Working Condition-
Full time position.
Participation in ongoing training & development program.
Email-
