Clinical Data Manager Apprenticeships are 18-24 month commitments designed to help life sciences companies better collect data and improve their reproducibility in research.

We use grants through our foundation to cover the costs of training and mentorship. This includes practical, on site instruction at a host company in areas such as clinical trial team support, collection of essential clinical trial data, data entry, queries and resolution, data verification, data maintenance, assistance in the operational and logistical aspects of clinical trials. Complementary topics such as introduction to good clinical practices and electronic data capture, clinical trial data oversight and support, laboratory and medical terminology, industry regulatory guidances and a recognized industry certification.

Clinical Data Apprentices at Allergan

Nine clinical data apprentices working at Allergan through the MEIRxRS

This 18-24 Month apprenticeship includes the goal of becoming an employee upon completion of program. If you are unable to directly hire the apprentice at the end they can be converted to a staffing arrangement or we can help them find a new position. Apprentices can be military veterans, students/recent graduates, mothers or fathers returning to the workforce or individuals coming off disability.

Responsibilities in Clinical Data Manager Apprenticeships

Clinical Data Managers are responsible for collecting data from clinical trials created for pharmaceuticals, biologics, or devices. They ensure data collected is accurately, grouped properly, solve operational problems, and may prepare statistical reports. They work with complex computerized records systems and maintain security and integrity. Each apprenticeship opportunity includes a certification upon completion.

• Collect data from clinical trials.
• Sort information and then ensure it is screened, grouped, summarized, transcribed, and coded.
• Consult with other employees to solve operational problems.
• Provide clerical duties such as entry, transcription, coding, and collating searches.
• Prioritize work in line with project management decisions.
• Manage clinical trials through review, computerization, cleaning and auditing of clinical and safety data and databases in compliance with standard operating procedures, client guidelines and regulatory agency guidelines.
• Validate clinical trial data to ensure consistency, integrity and accuracy based on project specific guidelines.
• Generate data retrievals and summaries.
• Query data inconsistencies and revise case report forms in compliance with standard operating procedures. Perform query resolution and initiate direct contact / follow up with sites for additional information.
• Review case report forms for completeness and consistency.
• Implement strategy for data cleaning and the design and programming of clinical databases.
• Review and approve design, review ground rules and database design according to Standard Operating procedures and protocol.

Included Instruction

• Work with complex computerized records systems and maintain security and integrity.
• Collect data from clinical trials.
• Sort information and then ensure it’s screened, grouped, summarized, transcribed, coded.
• Prioritize work in line with project management decisions.
• Provide clerical duties such as data entry, transcription, coding, and collating searches.
• Manage clinical trials through review, computerization, cleaning and auditing of clinical and safety data and databases in compliance with standard operating procedures, client guidelines and regulatory agency guidelines.
• Validate clinical trial or safety data to ensure consistency, integrity and accuracy based on project specific guidelines.
• Generate data retrievals and summaries.
• Query data inconsistencies and revise case report forms in compliance with standard operating procedures. Perform query resolution and initiate direct contact / follow up with sites for additional information.
• Review case report forms for completeness and consistency.
• Implement strategy for data cleaning and the design and programming of clinical databases.
• Review and approve design, data review ground rules and database design according to Standard Operating procedures and protocol
• Consult with other employees to solve operational problems.

Find out more

Employers interested in Clinical Data Manager Apprenticeships should contact us using the form down below.

If you are interested in starting your career in one of our Clinical Data Manager Apprenticeships then submit your resume on our page for Prospective Apprentices.

Contact Us

Interested in working with us? Reach out below.

100 N. Brand Blvd, Suite 306
Glendale, CA 91203
818-247-1368
info@meirxrs.com
sales@meirxrs.com

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