www.gratisol.com Labs India Hyderabad : Clinical Research Training

[gratisollabs]

GRATISOL LABS a leading Clinical Research training and recruitment center based in Hyderabad provides 2 months CCDM (Certificate Clinical Data Management) job training course with 100% placement assistance.

Gratisol Labs LLC is a UK based healthcare Industry supporting Bio pharmaceuticals with customized Bio informatics solutions and contract research services. Gratisol Labs LLC also involved in the R&D, commercial production and marketing of Bio pharmaceutical products all over the world.

Apart from Industry Services, Gratisol Labs LLC is providing advanced Certified Training Program in Clinical Data Management, Bio statistics and Bio informatics with ORACLE CLINICAL 4.6 certification to help the Healthcare Graduates to settle in the industry. Trainees get practical exposure apart from Project/Training. The program offers hands on training experience to create career paths with combination of our training framework and collaborative effort with the industry.

The following modules are covered in this certification program :
Introduction to Databases
Data management Plan
Study set up
Electronic Data Capture
CRF Design
Pharmacovigilance
Regulatory Aspects in Pharmacovigilance
Adverse Drug Reactions (ADR)
Management of ADR
Medical Evaluation of ADR
Periodic Safety Update Reports
MedDRA
EudraVigilance
Oracle Clinical, Rave

Eligibility :
• Any Graduate and Post Graduate in Medical and allied fields like Dentistry, Homeopathy and Pharmacy.
• Any Graduate and Post Graduate in Biological Sciences, Biotechnology, Nursing, Physiotherapy, Occupational therapy and Social sciences.
• Applicants Currently Engaged in Clinical Research, Institutions and officials engaged in Clinical Research

For further Information/guidance, please send your enquiry by email to training@gratisol.com
For Further Information/Guidance/Enrollment Please Feel Free To Call 040-65741017, 08885198390

Contact Details :
Gratisol Labs India(Andronovo Labs Training Partner)
Plot No. 70, 3rd Floor,
Road No. 10, Banjara Hills
Landmark : Star Hospitals/Mandir Showroom
Hyderabad – 500034
Phone : +91-4065741017
Mobile :+91-8885198390
E-mail :training@gratisol.com
Website : http://gratisol.com/

[Guest]

Clinical Research Professional with 1 year of experience seeking further growth in the clinical research industry
Keerthi Mundhra
Email : keetu.apr10 AT gmail.com
Career objective :
Seeking a challenging role in a professional organization, that offers value addition to both the organization as well as my personal profile, fully utilizing my skills and abilities. Area of interest includes clinical operations and PV.
Academic profile
Pursuing Post Graduate Diploma in Clinical Research from James Lind-Global Research Academy (2011)
Achieved Graduation degree in Pharmacy from Kakatiya University with Distinction (2006-09)
Professional experience
Core training
- Was guided on ethics involved in clinical research
- Was instructed about the roles and responsibilities of clinical research personnel
- Was instructed on study start up, monitoring, compliance and audits involved in trials
- Was guided on project and vendor management, also financial aspects involved in trial
- Was taught about personality development and communication skills incuding time management and conflct management as a part of curriculum
- Was introduced to clinical data management and pharmacovigilance aspects.
Internship Experience (01/06/2011 to 30/11/2011) :
As part of my internship I have performed the following task meeting the given timelines.
- Protocol Writing : Developed the protocol as per the ICH GCP, 21 CFR and Indian GCP.
- Budget Preparation : Prepared the budget for the Study as well as the Site.
- CRF design : Designed the CRF capturing all the study events as per the protocol requirements.
- Source Document and Subject Diary : Prepared the socurce document and also subject diary capturing the treatment and study assessments as per the potocol.
- ICD : Prepared the informed consent form and the Patient Information Sheet as per Schedule Y and ICMR Ethical Guidelnes for Biomedical Research.
- Logs, Forms and Reports : Prepared the study specific logs, forms and reports.
- SIV, Monitoring, Close out visits : Performed mock initiation, monitoring and close out visits of the study.
- Prepared and submitted EC dossier
- Completed CRF’s and other study related documents using dummy subject data.
- Compiled and maintained the TMF’s and ISF’s
Seminars and workshops
- Presentation on protection of human subjects in clinical trials in Global Hospitals, Hyderabad
- Presentation on Euthanasia in Global Hospitals, Hyderbad
- Attended webinar on clinical Trials : Asia-Pacific speaker NADINA C.JOSE, MD Former director for global Clinical Site management and monitoring for the Asia –Pacific region, Allergan Inc, USA
- Participated in youth empowerment and skills workshop (YES+)
Extra curriculur activities
- Worked as volunteer for art of living organization
- Participated in district level science fair exhibition and won first prize
- Experience as leader of college organization

[harika p]

HARIKA P
Email : harikap.anu AT gmail.com

Career Objective :
To implement my knowledge and skills to build a career in the field of clinical research thereby proving profitable for the organization.
Academic Qualification :
- Advanced Post Graduate Diploma in Clinical Research and Management from Clinical Research Education and Management Academy (CREMA) affiliated to Jaipur National Universisity.
- Graduation in life sciences with Biotechnology ,Chemistry, Zoology from J S S College, Karnataka University, Dharwad with distinction 80.22%.
- Pre university education (M. Bi. P.C) from K L E Preuniversity college, Karnataka with first division .
- Schooling from Bethel English Medium School, Karnataka with first division.
Technical Skills :
- Working knowledge of MS Office.
- Life science graduate trained with Clinical Research, Pharnacovigilance and Clinical Data Management.
- Clinical Research
Drug Discovery and Development Process
ICH GCP
Pre Clinical and Clinical Trial phases.
Schedule Y
Regulatory Bodies-India, USA, Japan, EU, Australia

Pharmacovigilance
ICH E2A, E2B, E2C, E2D, E2E Guidelines
Adverse Event and Serious Adverse Event Reporting Time Frames
CIOMS
Narrative Writing
- Clinical Data Management
Data Management workflow process.
Case Report Form Development and Annotation
CDISC, CDASH, STDM .
Personal skills :
- Excellent organizational, communicative and problem solving skills.
- Accurate and valuable worker with successful work accomplishment.
- Excellent ability to accept and welcome new challenges.
- Ability to learn new procedures and skills with very good memory retention.
- Good in communicating and making my colleagues comfortable at work
Co-curricular Activities :
- Mini project on vermiculture.
- Participated in ” First Aid Nature Cure Training Course” .

[gratisollabs]

Gratisol Labs is a Clinical Research Organization (CRO) providing a broad spectrum of Clinical research, Clinical Data Management, Pharmacovigilance,CDISC SDTM, Bioinformatics & Genomics Corporate training & staffing services to the Global Pharmaceuticals, Biotech, CROs, Medical device, IT/ITeS Organizations, Clinical sites, Hospitals & Healthcare Organizations globally.

Oracle Clinical
Oracle Clinical provides the life science industry with an integrated Clinical Data Management (CDM) and Remote Data Capture (RDC) application on the market. Oracle Clinical was built based on the extensive experience of hundreds of companies that conducted clinical trials—which gives Oracle Clinical an essential industry perspective. Unlike other vendor offerings, Oracle Clinical provides single application architecture for both CDM and RDC. Oracle Clinical provides additional functionality in key areas such as integration, data collection, localization, and reporting.

New Batch Starts Every Monday. We also provide support in client interviews; resume preparation, and ticket resolving. We also offer free H1 processing for OPT's & H4 visa holders along with accommodation and placement services. Hostel facility arranged if some one interested to join classroom training in Hyderabad.

For further Information/guidance, please send your enquiry by email to training@gratisol.com.

Contact training@gratisol.com to register for a free demo and course contents.

For Further Information/Guidance/Enrollment Please Feel Free To Call 040-65741017, 08885198390

Contact Details:
Kunal Singh
Manager – Hr & Staffing

Gratisol Labs
Plot No: 70, 3rd Floor,
Road No-10, Banjara Hills,
Landmark: Near Star Hospitals
Hyderabad AP – 500034
Contact No: 040-65741017,8885198390
E:mail: hr@gratisol.com, training@gratisol.com
Website: www.gratisol.com

[Guest]

Respected sir/madam, please accept my resume.