Karthik Ramasamy
Trial Related Experience: • Informed Consent Process, Screening and Enrollment of study subjects. • Maintaining Site Master Files • Interactive Voice Response system (IVRS)... | India
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Karthik Ramasamy’s Emails ka****@ic****.com
Karthik Ramasamy’s Phone Numbers No phone number available.
Social Media
Karthik Ramasamy’s Location India
Karthik Ramasamy’s Expertise Trial Related Experience: • Informed Consent Process, Screening and Enrollment of study subjects. • Maintaining Site Master Files • Interactive Voice Response system (IVRS) calling • Study Drug Accountability • Sample labeling and Dispatching • AE monitoring, reporting and follow up of study • IEC/IRB correspondence including SAE submission, all essential documents. • Managing all trial activities including site initiation, sponsor visit, auditor visits. • Maintain drug accountability, collect data, and report adverse events. • Understanding of Clinical Data Management process. Hands on experience of eCRF- Oracle, RAVE. • Data entries in CRFs, Validation, Data clarification forms and queries resolution.
Karthik Ramasamy’s Current Industry Icon
Karthik
Ramasamy’s Prior Industry
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E4e
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Apollo Hospital
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Smo Connect Clinical Research Service
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Apollo Hospitals Education And Research Foundation Chennai
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Apollo Hospitals Enterprises
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Iprocess Clinical Research Organization
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Work Experience
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Senior Clinical Research Associate
Sun May 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
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Clinical Research Associate Ii
Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Iprocess Clinical Research Organization
Clinical Research Associate
Wed Jun 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Apollo Hospitals Enterprises
Senior Clinical Research Coordinator
Tue Sep 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Apollo Hospitals Education And Research Foundation Chennai
Clinical Research Coordinator I
Sat Mar 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jun 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Smo Connect Clinical Research Service
Clinical Research Coordinator
Sat Dec 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Mar 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Apollo Hospital
Trainee- Clinical Research Coordinator
Wed Aug 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Nov 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
E4e
Medical Coder
Thu Jul 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Dec 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time)
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Senior Clinical Research Associate
— PresentSkills
Languages
Karthik Ramasamy Email Addresses
FAQ About Karthik Ramasamy
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Karthik Ramasamy is located at
India -
Karthik Ramasamy is a
Trial Related Experience: • Informed Consent Process, Screening and Enrollment of study subjects. • Maintaining Site Master Files • Interactive Voice Response system (IVRS) calling • Study Drug Accountability • Sample labeling and Dispatching • AE monitoring, reporting and follow up of study • IEC/IRB correspondence including SAE submission, all essential documents. • Managing all trial activities including site initiation, sponsor visit, auditor visits. • Maintain drug accountability, collect data, and report adverse events. • Understanding of Clinical Data Management process. Hands on experience of eCRF- Oracle, RAVE. • Data entries in CRFs, Validation, Data clarification forms and queries resolution. Icon -
Karthik Ramasamy currently works in the
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Karthik Ramasamy specializes in
Trial Related Experience: • Informed Consent Process, Screening and Enrollment of study subjects. • Maintaining Site Master Files • Interactive Voice Response system (IVRS) calling • Study Drug Accountability • Sample labeling and Dispatching • AE monitoring, reporting and follow up of study • IEC/IRB correspondence including SAE submission, all essential documents. • Managing all trial activities including site initiation, sponsor visit, auditor visits. • Maintain drug accountability, collect data, and report adverse events. • Understanding of Clinical Data Management process. Hands on experience of eCRF- Oracle, RAVE. • Data entries in CRFs, Validation, Data clarification forms and queries resolution. -
Karthik Ramasamy speaks the following languages:
No languages available. -
Karthik Ramasamy has prior experience in the following industries:
Iprocess Clinical Research Organization , Apollo Hospitals Enterprises , Apollo Hospitals Education And Research Foundation Chennai , Smo Connect Clinical Research Service , Apollo Hospital , E4e -
Karthik Ramasamy has the following professional experience:
Icon , Icon , Iprocess Clinical Research Organization , Apollo Hospitals Enterprises , Apollo Hospitals Education And Research Foundation Chennai , Smo Connect Clinical Research Service , Apollo Hospital , E4e , Icon . -
You can view Karthik Ramasamy’s
LinkedIn profile at LinkedIn URL. -
Karthik Ramasamy’s work email addresses are
[email protected] . -
Karthik Ramasamy works at
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