Dear Candidate
Job Title : Sr. Research Associate/Associate Scientiest(Clinical Research Physician)
Experience- Fresher or Having 1-3years of Experience in Clinical Trials.
Job Responsibilities :
Protocol, Informed Consent From (ICF), case report form (CRF) Preparation:
· Coordinate with clinical research personal for of Protocol.
Coordinate with clinical research personal for preparation of ICF and CRF
Ethics submission :
Coordinate with the investigator for submitting the study related documents (clinical updated) to independent Ethics Committee.
Subject Recruitment/ Screening :
Coordinate with screening team for subject recruitment & screening.
Study Related :
· Coordinate with the investigator for planning of study schedule.
· Ensure that all the volunteers reported for ICF presentation are fit for participation in the study as per the respective protocol.
· ICF presentation at the time of participation of subjects in a particular study.
· Conducting clinical examination and monitoring vitals for well-being of subject during the study.
· Responsible for safety and well being of study subjects.
· Handling & Reporting of adverse events and drug reactions and clinical emergencies in co-ordination with investigator.
· Clinical decision in the absence of investigator and take opinion of investigator as and when required.
· Guide the nursing staff in maintenance of emergency medicines and special care room.
· Provide medical help to the employees as well as subject.
Monitor the study and ensure that the study is conducted as per approved protocol, international conference on harmonization – Good clinical Practice (ICH-GCP) and on house standard operating procedure. (SOP)
· Coordinate with clinical staff for admission, discharge, meal distribution dosing/ dosing supervision and monitoring the subjects during study for restriction compliance.
Generation and maintenance of essential documents preparing to study.
Report preparation:
List out protocol deviations/ SOP deviations related to clinical examination and vital measurement and incorporate the same in final report in consultation with the investigator.
Feasibility assessment :
Coordinate with the clinical research for feasibility assessment of various molecules .
Kindly send us your updated CV with current CTC & expected CTC if interested.(Urgent opening)
Regards,
Pooja Chavda
Switchover Solutions
12/A Sarthik , 2nd Floor,
Beside Gulmohar park Mall,
Satellite Road, Ahmedabad - 380015.
pooja@switchover.in
079 40030004
www.switchover.in
Job Title : Sr. Research Associate/Associate Scientiest(Clinical Research Physician)
Experience- Fresher or Having 1-3years of Experience in Clinical Trials.
Job Responsibilities :
Protocol, Informed Consent From (ICF), case report form (CRF) Preparation:
· Coordinate with clinical research personal for of Protocol.
Coordinate with clinical research personal for preparation of ICF and CRF
Ethics submission :
Coordinate with the investigator for submitting the study related documents (clinical updated) to independent Ethics Committee.
Subject Recruitment/ Screening :
Coordinate with screening team for subject recruitment & screening.
Study Related :
· Coordinate with the investigator for planning of study schedule.
· Ensure that all the volunteers reported for ICF presentation are fit for participation in the study as per the respective protocol.
· ICF presentation at the time of participation of subjects in a particular study.
· Conducting clinical examination and monitoring vitals for well-being of subject during the study.
· Responsible for safety and well being of study subjects.
· Handling & Reporting of adverse events and drug reactions and clinical emergencies in co-ordination with investigator.
· Clinical decision in the absence of investigator and take opinion of investigator as and when required.
· Guide the nursing staff in maintenance of emergency medicines and special care room.
· Provide medical help to the employees as well as subject.
Monitor the study and ensure that the study is conducted as per approved protocol, international conference on harmonization – Good clinical Practice (ICH-GCP) and on house standard operating procedure. (SOP)
· Coordinate with clinical staff for admission, discharge, meal distribution dosing/ dosing supervision and monitoring the subjects during study for restriction compliance.
Generation and maintenance of essential documents preparing to study.
Report preparation:
List out protocol deviations/ SOP deviations related to clinical examination and vital measurement and incorporate the same in final report in consultation with the investigator.
Feasibility assessment :
Coordinate with the clinical research for feasibility assessment of various molecules .
Kindly send us your updated CV with current CTC & expected CTC if interested.(Urgent opening)
Regards,
Pooja Chavda
Switchover Solutions
12/A Sarthik , 2nd Floor,
Beside Gulmohar park Mall,
Satellite Road, Ahmedabad - 380015.
pooja@switchover.in
079 40030004
www.switchover.in
