TARLOK ATWAL

31 Cherrytree Drive Brampton, Ontario L6Y 3L6, Canada

Phone: (905) 459-7517 Cell: (416) 845-7517 E-Mail: ta966bd2@westpost.net

Objective: To obtain position as Clinical Research Associate

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PARSONAL PROFILE
a Pleasing personable, friendly, well organized, reliable and accountable
a Proven capability of handling work independently with minimum supervision
a Multitasking ability with attention to detail and work under pressure to compl
ete projects on time
a Proven interpersonal skills for creating liaison, trust, friendships and colla
borative relationships
a Outstanding verbal, written & telecommunication skills in appropriate & timely
manner
a Flexible and willing to learn & accept new jobs and apply in different situati
ons
QUALIFICATIONS
a Capable of conducting trial related activities; site selection, initiation, t
raining, monitoring & close out
a Performing specific duties & tasks according to Protocols, ICH- GCP, SOPs and
regulatory requirements
a Good knowledge of clinical diagnostics, therapeutics & procedures for various
diseases and disorders
a Monitoring trial sites for performance and data verification for accuracy, val
idity and completeness
a Timely review and completion of all SAEs ensuring appropriate action
a Efficient performance of product accountability and supply tracking, trial bud
geting and planning
a Comprehensive knowledge of drug and device development process and stages in c
linical research
a Proficient in computer skills for MS Office, Word, Excel, Outlook, Power Point
& online applications
a Ability to travel over 80 % of time as per study requirements
EDUCATION
a Post Graduate Diploma with, ICH/ GCP Certification in Clinical Research
a Graduate Degree in Medical Sciences
a Internship in Clinical Research
RELEVANT SKILLS AND EXPERIENCE
GRPC, Toronto Ontario Canada
(Sep-Nov 2010)
Working on New Product Study Initiation & Documentation Process
Preparing study Schedules, Procedures, protocol, information materials, CRFs and
ICFs
Academy of Applied Pharmaceutical Sciences (AAPS), Toronto Ontario, Canada
(Sep 2009-July 2010)Worked on various Clinical
research Projects, which include;
a Designing and preparing study related documents such as, protocols, consent fo
rms, CRFs, investigator Brochures and other study related materials

a Preparing study specific Applications & document packages for REB and regulato
ry submission
a Assisting in drafting, proofreading manuscripts, preparing periodic, annual an
d final study reports
a Active coordination and management of all study related activities from site s
election to site close out as well as participating and conducting trainings.
Family physician: New Delhi,India
(Before-1999)

a Responsible for diagnosis, treatment, long-term follow-ups, comprehensive and

continuous care for patient.
Other Employment Related Experience

Product Distributor: in Canadian Tire Distribution Centre in Brampton Ontario,

Canada (2008-2009)
Systems Operator: (Automotive Industry), Ontario Canada
(2000-2008)
System of Precision measurements & statistical -correlations for Solution Implem
entation
PROFESSIONAL EDUCATION AND TRAINING
Post Graduate Diploma with ICH-GCP Certification Clinical Research
(Sep 2009-July 2010)
Internship in Clinical Research:
From GRPC Toronto Ontario, Canada
(Sep 2010-Onward
s)
Graduate Degree in Basic & Clinical Sciences:
From All India Institute of Medical Sciences & Research (AIIMS) New Delhi, India
Clinical Epidemiology: WHO and Infectious diseases directorate, Delhi, India
Standard First Aid, CPR & AED Certification: Red Cross Canada
(April 2010)
Very well trained with extensive experience in Phlebotomy

GOALS: To be an asset for the organization I am going to join and work for its g
rowth and prosperity
MEMBERSHIPS:
Active member of
1. Society of Clinical Research Associates (SOCRA)
2. American Medical Writers Association (AMWA)
3. Clinical Research Institute of America (CRIA)