Position : Clinical Research Education: · A graduate or post-graduate with science &/or medical &/or pharmaceutical back ground. · Diploma &/or degree in Clinical Research. JOB Responsibility: Assist in the compilation of all trial related documents during the pre-trial
CDM experience and can work effectively in big teams. Should have exposure to discrepancy. InForm or Rave knowledge mandatory PS: DO NOT SHARE ORACLE CLINICAL EXP CANDIDATE. Work Location:- Mumbai Night Shift/ Rotational Shifts:- Yes B. Sc / B. Pharm/M.Sc /M. Pharm Not more than 3 years of experience for B. Pharm/ B. Sc & 2 years in case of M. Pharm / Msc
resolution. 8. Help in Protocol specific sample collection & shipment of Lab samples and IP. 9. Other Miscellaneous activities like documentation, record keeping, IP Accountability etc. 10. Safety reporting of Clinical research participants and compile & submit CIOMS and Appendix XI ...
information back to research team members. Coordinates with PIs and department to help ensure that clinical research and related activities are performed in accordance with Federal regulations, BFS and sponsoring agency policies and procedures. Assists the PI in development of materials and tools
reports. Mumbai, Mumbai Pune, Pune
"While going for interview please mention you got this reference from Aasaanjobs"We are looking for candidates who are willing to work in mumbai as data collector, where candidates will visit pet shops, veterinary clinics, kennel etc. and gather the required data and perform analysis on accumulated
and marketing plans.2) How to approach the place? How to approach vendors?3) Form and basic guidance of website.4) Vendors benefitTarget area : pet care industry in Mumbai.1) Kennels or hotels2) Pet shops3) veterinaries4) Grooming salon5) NGOs or adoption centers Mumbai, Mumbai
Medical Coding Role & Responsibility: -The process to cut short patient medical reports into alphanumeric codes for easy insurance claim Clinical Research Role & Responsibility: -Process of testing new medicines and to conduct trials. Pharmaco Vigilance Role & Responsibility: -The process
the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to relevant stakeholders and/or line manager. Coach junior clinical process associate/specialists Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and ...
into category segmentation, total cost of ownership, strategic and operational risk and compliance and contract analysis. Establish reporting against contract renewals and compliance Salary: Not Disclosed by Recruiter Industry: Pharma / Biotech / Clinical Research Functional Area: Accounts, Finance ...
entities around the world. The Global Knowledge Network is an integrated specialist team that helps facilitate deals and transactions globally by working directly with our investment bankers, sales, traders and research analysts from around the globe. Position Overview This role will be responsible
Your role will include: • Researching and identifying potential business partnerships • Reaching out to current partners and developing new opportunities • Helping to shape the overall business strategy and entering into strategic alliances with potential business partners Qualifications Ideal
for quality assurance studies. Actively participate in presentations of CMEs and Journal clubs. Assist the consultant To complete patient history form, visit patient and review medical record. Obtain relevant clinical information for inclusion in report.. Assists the Consultant for: o Special material
the Consultant for: Special material management requirement Ensure quality of performance of the department In all emergency cases in scheduling of cases and coordinating the department activities To co-ordinate the Inter and Intra-departmental activities in research, camps, presentations, referral reply
as part of quality assurance studies. Gather data for quality assurance studies. Actively participate in presentations of CMEs and Journal clubs. Assist the consultant To complete patient history form, visit patient and review medical record. Obtain relevant clinical information for inclusion in report.. Assists
medical record. Obtain relevant clinical information for inclusion in report.. Assists the Consultant for: o Special material management requirement o Ensure quality of performance of the department o In all emergency cases o in scheduling of cases and coordinating the department activities o