SJRI D Pharma Job – Clinical Research Coordinator – Sanofi Project

SJRI D Pharma Job – Clinical Research Coordinator – Sanofi Project

SJRI D Pharma job opening 2023, Clinical Research Coordinator job opening 2023, Clinical Research Coordinator job opening 2023, Pharmacy job opening in Sanofi Paediatrics Study Project, Candidates with a diploma degree in pharma may apply for the job opening. Interested and eligible candidates may check out all the details

Job Title: Clinical Research Coordinator – Sanofi Paediatrics Study Project

Division Non-Division User

Project / Title Sanofi Paediatrics Study Project

Contact Person Mrs. Lincy ThomasContact No080-49467010/7011/7021

Job Details

Brief Description about the Project

Responsible for multiple studies and specifics as per the protocols submitted to IEC.

• Interaction with Patients, Sponsor/CRO, IEC, Lab staff and other departments in the institution and conduct the study according to ICH GCP Guidelines, SOPs’ and study protocol guidelines and act as the main line of communication between patients,
• Investigators and CROs in study conduct activities.
• Assist in Feasibility questionnaires, Coordinate in pre-site selection visit, site initiation visit.
• Assist the Principle Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing studies
  Clinical Research Coordinator

Position Starting: 01st February 2023

No. of Vacancy: One

Employment status:

Salary: Rs 20,000/-pm to be escalated depending on job performance

Preferred Qualifications:  Pharm D,

Language: English, Kannada, Telugu, Tamil

Experience: 2-3 years

Last Day for Receiving Application: 24th January, 2023

Roles and Responsibilities:

• Coordinate in screening, Audio-Video consenting, enrolment, periodic study visits and close out visit.
• Ensure that rights and well being of a research participant is protected throughout the duration of the study.
• Coordinate with finance, legal and regulatory team and assist in the preparation of CTAs specific to the trials.
• Assure all study documentation is maintained by completing the source documents for each
• Patient and maintaining and updating Site Master Files.
• Completing CRFs, e-CRFs on time and resolve data queries.=
• EDC, InForm & Medios data capture.
• Ensure and maintain inventory of Study consumables like Investigational product handling, storage, dispensing, accountability, tracking temperature, calibration of equipments, sample centrifugation, courier of documents and lab samples shipment.
• Timely preparation, notification and tracking of the Ethics committee submissions.
• Submission of the study progress, amendments, Protocol Deviations, AE’s and SAE’s to the ethics committee and sponsor in a timely manner.
• Coordinate with the investigator and the safety monitoring team at the time of SAEs.
• Assist in resolving IEC, DCGI and FDA queries.
• Coordinate and participate in monitoring visits with sponsor/CRO and Facilitating inspections/audits.
• Follow up with patients and document in telephone contact report.
  Conduct study closeout visit and archive the documents.
• Maintain record of closeout studies and resolve the post closeout queries.

How To Apply:

Interested candidates may send their Resume to:

The Principal Investigator

Atlas Paed and Neo Atlas /other Hemophilia Studies Project

SJMCH

To Apply: E-mail cover letter and curriculum vitae with 3 references (names and email addresses/phone numbers) by on or before 24th January, 2023 to [email protected] & cc to [email protected].

For more information, please visit our website www.sjri.res.in

Can Contact us on the following Numbers 080-49467010/49467011/49467021

Last Date To Apply: 24th Jan 2023

Click Here To Apply Now

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