1. CCURRICULUMURRICULUM VVITAEITAE
OOBJECTIVEBJECTIVE
To maximize the potentials and utilize them effectively to attain organizational
goals and objective through positive attitude, flexibility and open mindset. To
enhance knowledge for professional growth in the field of clinical research and
elevate to higher achievements in career and procure responsibilities that account on
the basis of performance and diligent work.
PPROFILEROFILE
• 2 + years’ experience in the field of Clinical research
• Trained on ICH-GCP and with Regulatory Guidelines.
CCURRENTURRENT PPROFESSIONALROFESSIONAL EEXPERIENCEXPERIENCE
Organization and Location: Apollo Hospitals Education and Research Foundation.
Duration: 07th
September 2015 to till date
Roll/Designation: Senior Clinical Research Coordinator
Organization and Location: Apollo Hospitals Education and Research Foundation.
Duration: 11th
March 2014 to till date
Roll/ Designation: Clinical Research Coordinator- I
Organization and Location: SMO connect Clinical Research Services Pvt Ltd
Duration: 12th December 2012 to March 10th
2014
Karthik.R
No 16, 2nd
cross,
Ragavendra garden,
Thiruvanaikovil,
Trichy-620008
Mob No:+91-8760344883/ 9886351987

2. Roll/Designation: Clinical Research Coordinator
Organization and Location: Apollo Hospitals Education and Research Foundation.
Duration: 26th
March 2012 to 7th
December 2012
Roll/ Designation: Trainee Clinical Research Coordinator
• Therapeutic areas
o Nephrology
o Diabetology
o Cardiology
• Phases of studies – III & IV
CURRENT JOB ACTIVITIESURRENT JOB ACTIVITIES
1. Informed Consent Process, Screening and Enrollment and Follow-up of
study subjects.
2. Trial Management from Feasibility till Study Close Out
3. Interaction with Investigators and Patients
4. Maintaining Site Master Files
5. IP Accountability, Sample labeling and Dispatching
6. AE monitoring, reporting and follow up of study
7. IEC/IRB correspondence including SAE submission, all essential
documents.
8. Managing all trial activities including site selection, site initiation Visit and
study close out.
9. Understanding of Clinical Data Management process. Hands on experience
of eCRF- Oracle, RAVE, Inform and United therapeutics
10. Performing IVRS/IWRS- Clinphone, Cenduit system
11. Data entries in CRFs, Validation, Data clarification forms and queries
resolution.
12. Maintaining Different logs and Site files
13. Serious Adverse event management
14. ICF & CRF preparation for the Investigator Initiative Studies.
15. Training the study personals and new employees on all trial related
activities.
Academic:
1. Teaching faculty for the clinical research course being conducted at
Apollo hospitals in collaboration with Anna University.

3. Topics Taken:
o Informed Consent Process
o Source Documentation
o Case Report Form
o SAE Management
2. Providing Hands on training to the students in applied clinical research
theory and practical classes
3. Training the interns in site related study specific activities
4. Token of appreciation from sponsor for making the site one of the
highest enroller
CLINICALCLINICAL TRIALSTRIALS INVOLVEDINVOLVED
ACADEMICACADEMIC QUALIFICATIONQUALIFICATION
DEGREE
DEGREE
GRANTING
UNIVERSITY /
SCHOOL
YEAR OF
PASSING
PERCENTAGE
Post Graduate Diploma ACC CTM (AU-KBC 2012-2013 Completed
Indication Phase Of
Studies
Sponsor CRO
Acute coronary
Syndrome
Phase III Novartis Novartis
Acute coronary
Syndrome
Phase III Covance Covance
Osteoarthritis in knee Phase III Troikaa Pharmaceuticals Limited
Pulmonary Artery
Hypertension
Phase III United
Theraputics
PRA Health
Science
Invitro Fertilization Phase IV Bharath serum Siro
Pharmaceutical
Invitro Fertilization Phase III ABBOTT PRA Health
Science
Diabetic study Phase III USV Apollo hospital
Arrthymias in CKD Device study Medtronic
PEPSICO study Observational Pepsico company and Apollo hospital
Lipotest Project Apollo Hospitals

4. in advanced clinical
research
Research Centre in
collaboration with
Apollo Hospitals
Educational Research
Foundation), Anna
University.
M.Sc(Biotechnology) SRM University 2008-2010 82%
B.Sc(Biotechnology)
Bharathidasan
University
2005-2008
72.4%
Higher Secondary
Govt Boys Higher
Secondary School,
Namakkal, Tamilnadu
2005
70%
High School
Bharathi High School,
Namakkal, Tamilnadu
2003
92%
WORKSHOPWORKSHOP && CONFERENCECONFERENCE ATTENDEDATTENDED
• “Overview on Clinical research in India, Monitoring in clinical research,
Quality improvement in Clinical trials and Audits & Inspections” conducted
by Sanofi, held at Apollo Hospitals, Chennai
• “Workshop on Pharmacovigilance Education Program” conducted by
Novartis, held at Apollo Hospitals, Chennai
• “Workshop on Medication Errors” conducted by Sanofi Aventis, held at
Apollo Hospitals, Chennai
• “Audits & Monitoring Conducted” by Sanofi, held at Apollo Hospitals,
Chennai
• “Designing Clinical Trials” conducted by Chettinad Hospital and Research
Institute.
• “Overview on Pharmacovigilance” conducted by Sanofi-Aventis.
• “Session on Pharmacovigilance” conducted by Sanofi-Aventis.
TECHNICAL SKILLS AND CERTIFICATES:
• Have done project on Phenotypic and Marker Assisted Evaluation of Grain
quality and Plant Growth Parameters in Rice, University of Agricultural
Sciences, GKVK, Hebal, Bangalore.
• Have done project on Pigmented Bacterial Diversity of Kakinada Mangrove
and its Characterization, MS.Swaminathan Research foundation,
Chennai.

5. SSTRENGTHSTRENGTHS
• Consistent performer as per the evaluation by the managers.
• Excellent inter-personal skills.
• Ability to prioritize, plan and work accordingly.
• Good Team player.
• Ability to adapt to the environment and to work in stress conditions.
• Excellent Verbal & Written Communication.
CCOMPUTEROMPUTER EEXPERIENCEXPERIENCE
• MS Word
• MS Excel
• MS Powerpoint
LLANGUAGESANGUAGES KKNOWNNOWN
PPERSONALERSONAL DDETAILSETAILS
Name : KARTHIK.R
Father’s Name : Ramasamy
Date of Birth : 10.06.1988
Gender : Male
Marital Status : Single
Nationality : Indian
Permanent Address : No 16, 2nd
cross, Ragavendra garden,
Thiruvanaikovil, Trichy-620005
Language Read Write Speak
English   
Tamil   

6. Contact Number : +91-8760344883/9886351987
DDECLARATIONECLARATION
I hereby declare that the above-furnished details are true and correct to the best
of my knowledge.
Place: Chennai
Date: 09 / June/ 2015 Karthik.R

7. Contact Number : +91-8760344883/9886351987
DDECLARATIONECLARATION
I hereby declare that the above-furnished details are true and correct to the best
of my knowledge.
Place: Chennai
Date: 09 / June/ 2015 Karthik.R