Clinical Data Management in Oracle Clinical OC/RDC Friday, 5 August 2016 No Comment

Job Summary



Locations:


Hyderabad / Secunderabad, Pune


Experience:


0 – 5 years


Keywords / Skills :


Clinical Research, Pharmacovigilance, Clinical Data Management, SAS Clinical, BDS, MSc, Bpharmacy, Mpharmacy, Pharm D, Fresher, Pharma, Trainee, training in Hyderabad, Jobs, Pharmacy, Pharmacist


Education:


BDS, B.E/B.Tech, BAMS, BHMS, B.Pharm, MBBS, M.E/M.Tech/MS, M.Pharm, M.Sc


Stream:


• Bio-Chemistry/Bio-Technology
• Environmental science
• Bio-Chemistry/Bio-Technology
• Environmental science
• Bio-Chemistry/Bio-Technology
• Biology
• Botany
• Chemistry
• Environmental science
• Microbiology
• Nursing
• Zoology


Function:


Pharmaceutical/ Biotechnology


Role:


Fresher


Industry:


• Bio Technology & Life Sciences
• Pharmaceutical


Summary:


BioMed Informatics Medwin Hospitals


Posted On:


4th Aug 2016








Online Training-Clinical Data Coordinator/Clinical Data Management in Oracle Clinical OC/RDC with Practical Hands on Training with Project 


BioMed Informatics Medwin Hospitals


(Established in the year of 2000) 


  • Before joining in BioMed Informatics Medwin Hospitals, You are welcome to check the appointment letters of our previous students issued by MNCs like Novartis, Quintiles, Accenture, Cognizant, TCS, Parexel International (India) Pvt Ltd, MakroCare, Synowledge and so on. 

  • We never make any phone calls to insist the candidates to join here by making empty promises. 

Online Training Features:

  • Globally Excellent demand & highly paid jobs 

  • Excellent opportunity to enter into this filed 

  • Web based classroom 

  • One faculty/student 

  • Placement support 

  • Flexible timings 

  • Regular/Fast track/Weekend batches 

  • Training Mode: Skype/Teamviewer 

  • Material will be provided 

  • Resume preparation tips / Interview guidance 

  • Practical Hands-on training on Database 

  • Direct access will be provided to Database 

BioMed Informatics Medwin Hospitals is a leading Clinical Research organization offering trainings since the year of 2000 that are helpful for Life Sciences/Pharmacy students to enter into IT Companies and Pharma, Biotech, CRO industries.


Hands on training will be provided on Oracle Clinical/RDC. Globally most of the Companies representing IT, Pharmaceutical, Biotechnology, SMO and Contract Research Organizations (CRO) have relied on Oracle Clinical to conduct Clinical Trials, making it the market-leading Clinical Research solution providing highly paid Oracle Clinical Jobs in India, USA, UK, as well as other countries.


Our candidates employed in Novartis, Quintiles, Cognizant, TCS, Parexel International (India) Pvt Ltd, MakroCare, Synowledge, Global Hospitals, Apollo Hospitals, NIMS, Glenmark Pharmaceuticals Ltd, Jubilant, Reliance Life Sciences, Shantha Biotechnics Ltd, Mahindra Satyam, SMO Clinical Research (I) Pvt Ltd, Pioneer Corporate Services Inc-USA, ICMR, AstraZeneca-UK, Texas Woman’s University-USA and many more…



Certification

Certificate will be provided for this course on successful completion of Assignments & Projects. Certificate would be awarded at the end of the program by BioMed Informatics Medwin Hospitals.


Interested candidates are kindly requested to fill Enquiry Form in the website www.biomedlifesciences.com for further information.




Contact:

G.V.L.P.Subba Rao


BioMed Informatics (Established in the year of 2000)


Medwin Hospitals B Block First Floor,


Nampally, Hyderabad – 500 001


Website: www.biomedlifesciences.com



Course Curriculum:

* Introduction to Clinical Research


* Introduction to Clinical Data Management


* Guidelines for CDM


* Roles and Responsibilities of CDM Team


* Clinical Data Management Process and Life cycle


* Data Management Plan


* 21 CFR Part 11


* CRF Designing


* CRF Annotation


* Data Capture Methods


* Data Entry


* Edit Checks


* Data Validation Procedures


* Discrepancy Management


* Data Clarification Forms (DCFs)


* Database Locking and Freezing


* Data Storage & Archival


* Data Coding and Medical Dictionaries


* SAE Reconciliation


* Quality Assurance & Quality Control


* Auditing


* CDISC Standards


Practical Hands-on Training on Oracle Clinical Database


INTRODUCTION:


* Introduction to OC window


* Subsystems in OC


STUDY PLAN:


* Defining Programs and Projects


* Defining Organization Units


* Defining Regions


* Defining Planned Studies


STUDY DESIGN:


* Easy Study Design


* Creating Intervals


* Creating Events


* Creating treatment patterns


* Creating Investigator, Site Records and Assignments


* Creating Patient Positions and Assignments


GLIB:


* Creating Questions


* Creating Question Groups


* Creating and Maintaining DVG’s


* Copy Groups


STUDY DEFINITION:


* Creating DCM’s, DCI’s & DCI Books


* Validation Procedures


* Derivation Procedures


* Test a Study


* Test Data Entry


DATA ENTRY:


* Initial Login


* Key Changes


* First Pass Entry


* Second Pass Entry


* Comparison Reconciliation


* Update


* Browse


* Patient Enrollment


* Missing DCMs


STUDY CONDUCT:


* Data Validation(Batch validation)


* Discrepancy Management


* Data Clarification Forms (DCFs)


* Data Extract and SAS Extract


* Making Mass Changes


* Locking and Freezing


LAB:


* Labs


* Lab Ranges


* Lab Units


* Lab test questions


* Lab Assignment Criteria


RDC (Remote Data Capture):


* Data entry in RDC


* Discrepancy Management in RDC


* Study and Site Security


You will be extensively involved in:


* Designing of electronic Case Report Forms (eCRFs) in Oracle Clinical


* Creation and maintenance of global library objects like DVGs Questions, Question groups, DCMs and DCIs


* Creating Data Collection Modules and layouts corresponding to CRFs to allow for data entry


* Generating and Testing data entry screens and validate the range, format, date, missing fields


* Conduct study start up activities, like Study design and Defining Sites, investigators and patients


* Creating, generating and testing Data Validation and Derivation procedures


* Writing edit checks or validation procedures using ranges provided or in accordance with the protocol


* Performing User Acceptance Testing (UAT)


* Data Entry like Initial Login, Key Changes, First Pass and Second Pass Data Entry, Comparison Reconciliation and Update


* Test and execute validation procedures (Both single and batch validation)


* Discrepancy management and Query management


* Generating queries based on validation checks to clarify and improve the quality of the data


* Creating DCFs and maintaining Discrepancies


* Resolving queries and updating the database.


* Review of un-resolved discrepancies, raise manual discrepancies wherever required and close where appropriate.


* Improving the quality of the data to ensure an error free, accurate data with no open queries


* Establishing and coordinating the timely completion of the database lock procedures.


* Reviewing clinical data as per SOP, protocol, and study specific guidelines


* Knowledge of Data Extract and SAS extract views


* Maintaining Lab ranges, Lab units, Lab test questions


* Data entry in RDC and Discrepancy Management in RDC






Clinical ResearchPharmacovigilanceClinical Data ManagementSAS ClinicalBDSMScBpharmacyMpharmacyPharm DFresherPharmaTraineetraining in HyderabadJobsPharmacyPharmacist




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Clinical Data Management in Oracle Clinical OC/RDC
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