Canvass Clinical Research Institute

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www.ccrsindia.

com
Our Vision...

- SWAMI VIVEKANANDA
Get it on
Play
Updated and organized Clinical Research
notes and LMS video library that are simple
to understand.
Ex. NDCT 2019 Guidelines

The institute's emphasis is on the syllabus


according to industry and Government
guidelines.
Ex. Guidelines required for DCGI
approval

Guidance for making a cover letter and a

CV, Giving personal attention to each

student during their SWOT analysis to enter

in clinical research industry.

Only institute which provides practical

approach for Project management, which you

cant even experience in 3 month's internship.

Institute Focuses on Updating the skillset of


the candidate to meet the need of the
recruiting companies.
Ex. Personality development and grooming
are provided by experienced professionals in
clinical research industry.
MS.Vijaya Bhakte
(Director, CCRSPL)

Armed with 17 years of work experience with

a pharmaceutical degree, and a diploma in

clinical research. Her objective is to offer

such clinical research training program

through which students may grow their

career in this field by increasing their mental

strength and expanding their skillset. Having

worked in the clinical research field for over

a decade and in all indications of clinical

studies as well as all phases of clinical trials,

she has an in-depth understanding of the

industry's expectations from Sponsors,

Contract Research Organizations, and

investigators. As a result of her experience

and clarity about industry expectations, the

CCRSPL students have an advantage over

their peers and counterparts.


Duration - 6 Months

Duration - 6 Months

Duration - 2 years
Duration : 2 yrs
Eligibility : B.SC (Life science Graduates)

Semester I
Anatomy and Physiology

Pathophysiology I

Pharmacology I

English Communication (Basic)

Semester II
Pathophysiology II

Pharmacology II

Clinical Trial Management I

Communications & Presentations

Semester III
Clinical Trial Management II

Clinical Data Management

Pharmacovigilance

SAS, Regulatory Affair , eTMF

Personality Development & Soft Skills

Semester IV
Internship in different segments of

Clinical Research (according to the

student inclination and their

performance)

Project Submission

Note* : 30,000 Rs for first three semester and 10,000 Rs for last semester.
Duration : 6 Months
Eligibility : BHMS, BAMS, BDS, B.pharma, M.pharma
Pharma D, B.tech(biotech)

Clinical trial management

Clinical data management

Pharmacovigilance

SAS (STATISTICAL ANALYSIS SOFTWARE)

Regulatory Affair

electronic Trial Master file

Soft skills and personality development

CV making and Interview technique.

Case studies based syllabus

Close monitoring to each student

Onsite training as per requirement of student

Video library of live sessions

100% Placement assistance

Discount can be availed by paying fees in

single installment.
Duration : 6 Months
Eligibility : M.sc (Life science)

Anatomy and physiology

Pathophysiology

Pharmacology

Clinical trial management

Clinical data management

Pharmacovigilance

SAS (STATISTICAL ANALYSIS SOFTWARE)

Regulatory Affair

electronic Trial Master file

Soft skills and personality development

CV making and Interview technique.

Case studies based syllabus

Close monitoring to each student

Onsite training as per requirement of student

Video library of live sessions

100% Placement assistance

Discount can be availed by paying fees in

single installment.
Clinical operation manager

Project manager

Clinical team leader

Inhouse Clinical Research Associate

Centralized Clinical Research Associate

Clinical research associate

Clinical research coordinator/Clinical trial assistant

Head pharmacovigilance

Pharmacovigilance physician

Safety expert

Medical monitor

QC/QA coordinator

Data analyst
Medical writer

Executives

Head - QA

Lead Auditor

QA executive

QA trainee/Assistance

Bussiness development manager

Executive
Head data management

Lead data manager

Assistant data manager

Validation programmer

QA/QC Coordinator

Clinical Data Management coder

Data Coordinator/Data Analyst

Head Regulatory affair

Manager

Assistant manager

Medical Advisor

Executive
Head Biostatician

Lead Biostatician

SAS programmer

Validation expert

Trainee Analyst

Centralised data moniter

eTMF Specialist
303-B Keshav imperial,

opposite shani mandir,

sitabuldi.

Nagpur 440012(MH)

766654529

8208448630

[email protected]

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