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Clinical Data Management
A Clinical Research is a systematic study for new drugs in human subjects to generate data for discovering or verifying the Clinical, Pharmacological (including pharmacodynamics and pharmacokinetic) or adverse Effects with the objective of determining safety and efficacy of the new drug.
Clinical Research Industry has grown around the world at an unparalleled rate in the past few years. It has opened up new vistas of employment for a large number of people. The Clinical Trials market worldwide is worth over US$ 45 billion and the industry has employed an estimated 2,10,000 people in the US and over 70,000 people in the UK and they form one third of the total Research and Development staff. These large numbers can be attributed to the fact that this industry offers lucrative employment opportunities. The average nominal annual salary growth across all the positions is 4% as against less than 1% for other segments.
Course Includes
40 Hours of Sessions
Flexible Schedules
24/7 Lifetime Support
FREE Demo on Request
One-on-One Doubt Clearing
Real-time Project Use cases
Instructor-led Clinical Data Analyst/ Manager live online Training Schedule
MAY 16 | WeekEnd | SAT & SUN (5.5 Weeks) | 07:00 AM to 10:00 AM (IST) ORIENTATION CLASS | |
MAY 18 | iuwegu | MON – FRI (15 Days) | 07:00 AM to 09:00 AM (IST) CLASS 1 | |
MAY 07th | WeekEnd | SAT & SUN (5 Weeks) | 08:30 PM to 11:30 PM (IST) CLASS 1 | |
MAY 09th | iuwegu | MON – FRI (15 Days) | 08:30 PM to 10:30 PM (IST) CLASS 1 |
MAY 16 WeekEnd | SAT & SUN (5.5 Weeks) 07:00 AM to 10:00 AM (IST) ORIENTATION CLASS | |
MAY 18 | MON – FRI (15 Days) 07:00 AM to 09:00 AM (IST) CLASS 1 | |
MAY 07th WeekEnd | SAT & SUN (5 Weeks) 08:30 PM to 11:30 PM (IST) CLASS 1 | |
MAY 09th | MON – FRI (15 Days) 08:30 PM to 10:30 PM (IST) CLASS 1 |
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Clinical Data Analyst/ Manager Job Description
Primary responsibility is to ensure the validity of clinical trial data and format them for statistical purposes. Also designs collection instruments, sets up databases and tracks and manages the flow of data to and from the investigative sites. With supervision, establishes protocol-specific data review and entry guidelines to document data validation and formatting procedures and defines batch-ending programs. Monitors timely data entry. Reviews data discrepancies resolutions provided by the investigative sites and enters corrections in the database, as appropriate. Assists in the review of interim/final data listings prior to transmission to other groups or inclusion in interim/final reports. Is familiar with database management systems and the principles, organization and content of standard Case Report Form (CRF) libraries. Ensures that incoming CRFs are tracked in a timely manner prior to safety review and upon manual review. Is familiar with data coding of Standard Operating Practices (SOP) and coding dictionaries. Conducts database audits according to established SOPs and is familiar with the implementation of GCPs.
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Realistic experience with real time project scenarios
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Task and assignments during the sessions
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