Anuj Kumar is a clinical research professional currently working as a Site Solutions Executive. He has over 5 years of experience working as a Clinical Research Coordinator on various clinical trials. His experience includes coordinating trial activities, ensuring protocol compliance, informed consent processes, data entry, maintaining documentation, and supporting site monitoring visits. He holds an Advanced Diploma in Clinical Research and degrees in Microbiology and Science. He is proficient in computer programs for clinical research and has participated in various clinical research training programs and workshops.

1. Page 1 of 3
CURRICULUM VITAE
CAREER OBJECTIVE
A dedicated Clinical Research Professional, with good
academic background, seeking a position that offers
professional growth in the field of Clinical Research to
utilize my skills and abilities.
“Ready for relocation anywhere in India for professional”
PRESENT ENGAGEMENT
Currently working as a Site Solutions Executive in Cytespace
Research Private Limited with Dr. Jasprakash Singh Grewal,
Senior Consultant/ Interventional Cardiology in SPS Apollo
Hospital, Ludhiana (May 2015 to till date).
WORK EXPERIENCE
 Worked as Clinical Research Coordinator with Dr.
Gurpreet Singh Wander, HOD & Chief Cardiologist in
Dayanand Medical College and Hospital, Ludhiana (April 2014
to April 2015).
 Worked as Clinical Research Coordinator Trainee under
the guidance of Dr. Gurpreet Singh Wander, HOD & Chief
Cardiologist in DMC&H, Ludhiana (Dec 2013 to Mar 2014).
PROFESSIONAL QUALIFICATION
 Advance Diploma in Clinical Research (One Year)
from Anovus Institute Of Clinical Research, Chandigarh
(PTU, Jalandhar) 2013
 Master of Science in Microbiology (MSc.) from H.N.B.
Garhwal University Srinagar Uttarakhand, 2011
 Bachelors of Science (BSc.) from C.C.S. University
Meerut, 2009
ICH GCP GUIDELINES TRANING
 Certificate of online ICH- GCP Guidelines training.
 Certificate of participation in ICH-GCP training
programe on “ICH- GCP” organized by Research &
Development Centre, DMC&H Ludhiana.
ANUJ KUMAR
E-mail Address :
anujrajyan14@gmail.com
Mobile No: +918437331863
+919410687198
Correspondence Address:
House No. 2648/1, Gurdev Nagar,
Near Aarti Chowk Ludhiana,
Punjab.141001
Permanent Address:
V/P.-Rangail, Tehsil-Nakur,
Dist.-Saharanpur, UP. 247341
Personal Detail:
Date of Birth : 2nd April 1991
Father’s Name: Sh. Parmod Kumar
Nationality : Indian
Sex : Male
Marital status: Married
Language Known:
English , Hindi , Punjabi
Strengths:
 Strong Interpersonal Skills
 Optimistic & Determined
 Dedicated & Hard worker
 Motivated & Self- driven by
competitions & challenges
 Extraordinary attention on details
 Excellent Problem solving Skills
 Good Team player and team
building spirit
 Good at multitasking &
Adaptable
 Excellent organizational and
demonstrated time management
skills

2. Page 2 of 3
WORK EXPERIENCE ON STUDIES
S. No. Indication of trial Clinical phase of
trial
(I-IV)
CRO
1. A Randomized, Double-Blind, Placebo-Controlled,
Parallel-Group Study to Evaluate the Effect of Alirocumab
on the Occurrence of Cardiovascular Event in Patient Who
have Recently Experienced an Acute Coronary Syndrome
IIIb
Ongoing
Sanofi
2. International Study of Comparative Health Effectiveness
with Medical and Invasive Approaches (ISCHEMIA)
An international
comparative
effectiveness study
iProcess
3. Effects of Yoga-based Cardiac Rehabilitation program
(Yoga-Care) on Cardiovascular health: a clinical trial
(India) and mechanistic study (UK)
Observational Study ICMR
4. Prospective Randomized On-X versus SJM Evaluation
Trial (PROSE)
Interventional iProcess
5. Asian Sudden Cardiac Death in Heart Failure a
Prospective Observational Study (ASIAN HF)
ASIAN HF Registry Quintiles
6. A prospective, multicenter, post marketing surveillance
study to evaluate the safety and effectiveness of the
Superia-Sirolimus Eluting Coronary Stent System
(SSECSS) implanted during routine clinical practice in
India
Phase IV Innvolution
Med
System
PROFESSIONAL EXPERIENCE
Current Roles and Responsibilities:
 To coordinate and facilitate all Clinical trial activities at site ensuring compliance with
protocol, applicable GCP guidelines and local regulations Informed consent process.
 Performs timely data entry of the Case Record Forms (CRF) or Electronic CRF (eCRF) in
consultation with the PI/ Investigator
 Maintaining clinical trial-related documents at site including Trial Master File.
 Preparing for, facilitating and assisting at site initiation, monitoring and close-out visits,
protocol-prescribed and other necessary patient-visits, QA visits, sponsor visits and
Inspections.
 Reporting site-performance metrics at pre-determined frequency.
 Coordinating submissions to ethics committee of protocol, adverse events and periodic study
reports for review and ensuring that all documentation to and from ethics committee is
appropriately maintained.
 Ensuring timely availability of IP and Lab kits and other clinical trial supplies and ensuring IP
is appropriately stored, maintaining temperature logs where necessary; also maintaining IP

3. Page 3 of 3
accountability and accurate record of all clinical trial supplies including lab kits; dispensing of
IP to subjects per the protocol under the supervision of the PI
 Assuring that all work at site prescribed by the approved protocol, the contract and the EC is
performed in a timely and comprehensive manner.
 Organizing and coordinating laboratory sample pick-ups and reporting.
 Assisting in timely resolution of data queries.
 Coordinating and supporting timely completion of protocol-related procedures by the PI,
specifically subject scheduling, subject screening and enrolment.
 Maintaining regular contact with site monitor regarding patient enrolment, visit scheduling,
dosing/ dispensing
 Supporting patient-awareness, training or other events at site or in the neighborhood
 Supporting data collection activity at site including but not limited to feasibilities,
epidemiological data.
COMPUTER PROFICIENCY
 Basics Knowledge of Computer.
 Familiar with Window ( XP, 7& 8), Microsoft Office (Word, Excel & PowerPoint).
 IXRS/IVRS, ORACLE, iMedidata
 Certificate of OC RDC (SITE) training.
TRAINING
 3 months training in Themis Medicare Limited Haridwar, (MAR 2011 to JUN 2011).
WORKSHOP
 Participation in EFC11570 –Odyssey Outcomes, Investigator’s Meeting 16th & 17th July 2016,
Delhi.
 Participation in EFC11570 –Odyssey Outcomes, Investigator’s Meeting 25th & 26th July 2015,
Mumbai.
 Certificate of participation in CME on “Basics of Cardiology” held at DMC&H Ludhiana.
 Certificate of participation in Workshop handling and demonstration of major instrument
required for Microbiological and Biotechnological Technique.
DECLARATION
I hereby declare that the information given above is genuine to the best of my knowledge & if you give an
opportunity to work in your organization, I will put my best efforts.
Place: Ludhiana (Anuj Kumar)
Date: 02-Aug-2016