Post Job Free

Resume

Sign in

Clinical Research Data Entry

Location:
Bangalore, Karnataka, India
Posted:
February 06, 2019

Contact this candidate

Resume:

ARUN KUMAR G

Marathahalli, Bangalore-****** (91-709******* ac8eyw@r.postjobfree.com

SUMMARY OF PROFILE

M. Pharmacy with exposure to Clinical Trials and Preclinical Trials.

A demonstrated track record of Clinical & Preclinical projects handling.

Looking for a career enhancement preferably with Pharma and Health care industries. AREAS OF EXPOSURE

Clinical Trials

Preclinical Trials

WORK EXPERIENCE

Medical Surveillance Specialist

IQVIA July 2015 – Oct 2018

Core Responsibilities:

Monitoring and evaluation of laboratory parameters for each patient at every site throughout clinical drug trial.

Lab listing review, discrepant data review, validation and safety documentation of trial patients.

Working with RAVE database, Clinical Data Quality control (CDQC) and eCRF locking systems.

Processing of Adverse Event (AE) reports through tracking, data entry, quality control, report generation and submission.

Project management and system support tasks.

Clinical Research Coordinator

St. Johns Research Institute (SJRI), Bangalore, India Jan 2015 – Apr 2015 Core Responsibilities:

Recruitment, coordination & follow up of trial subjects.

Covering informed consent, adhering to safety and compliance issues.

Sample collection, shipment and Clinical Data Management.

Adverse Events & Adverse Drug Reactions reporting to EC&CRO Sponsor promptly. INTERNSHIPS

Drug Safety Intern

Terzetto Pharma Metrics Private Limited, Bangalore. May 2015 – July 2015 Core Responsibilities:

Case study, Case processing and Med-DRA coding.

Maintaining the safety database and reporting systems.

Drafting case narratives and processing case-related information.

Responsible for end to end processing of spontaneous, solicited cases. Project Trainee (Pre-Clinical Research)

Sanzyme Ltd., Hyderabad, India Feb 2014 – Nov 2014 Responsibilities:

Drug Screening in Animal Models (In Vivo & In Vitro).

Pharmacodynamics, Pharmacokinetics (ADME) and Toxicity Studies.

Pharmacology of Drug Distribution status reporting.

Project Management and Productivity Tools (Trial Master File). CERTIFICATIONS

Microsoft® Office – 2007

ICH-Good Clinical Practice (GCP)

TECHNICAL SKILLS

Pharmacology and Toxicology of drugs

Knowledge of Phase I – IV Clinical trials.

ACADEMIC BACKGROUND

2014 M. Pharmacy-Pharmacology, (First class with Distinction) Jawaharlal Nehru Technological University Anantapur (JNTUA), Andhra Pradesh

2012 B. Pharmacy, (First class)

Rajiv Gandhi University of Health Sciences (RGUHS), Bangalore, Karnataka PERSONAL PROFILE

Year of Birth :1987

Gender /Nationality /Status :Male / Indian/ Married

Location preference :Bangalore/Anantapur

Languages Known :English, Telugu, Hindi, and Kannada PERSONAL STRENGTHS

Creative and innovative skills.

Written, verbal & presentation skills.

Work effectively with diverse groups of people.

DECLARATION

References are provided upon request.

Place: Bangalore

Date: 03/Jan/2019 (ARUN KUMAR)



Contact this candidate