Clinical Data Manager

An industry leading, international consulting company are looking to add highly skilled and experienced Clinical Data Manager to their team!

Job Overview:

The ideal candidate will have a strong background in the pharmaceutical industry, possessing either a bachelor's degree with a minimum of 3 years of relevant experience or be an experienced Registered Nurse (R.N.) with a preference for clinical research exposure. The Clinical Data Scientist must be detail-oriented, possess excellent communication skills, and demonstrate proficiency in various clinical data management tasks.

Responsibilities:

• Review of Clinical Trial Data: Evaluate Case Report Forms (CRFs), Monitoring Reports, and other relevant documents.
• Draft Listings and Tables: Collaborate in the creation and review of draft listings and tables related to clinical trial data.
• Query Resolution: Identify and propose queries to rectify inconsistencies or errors in completed Case Report Forms.
• Data Verification: Validate all data in the study database against information provided in relevant documents, ensuring accuracy and completeness.
• Review Comment Fields: Scrutinize comment fields in Case Report Forms for potential inclusion in study databases.
• Narrative Review and Preparation: Assess narratives for accuracy, completeness, and clinical relevance. Prepare draft narratives as required.
• Clinical Document Preparation: Contribute to the preparation of clinical trial reports and other essential clinical documents.
• Project Timeline Management: Take a lead role in managing project timelines, ensuring adherence to deadlines, and providing regular status updates to relevant stakeholders.
• Continuous Learning: Maintain and expand expertise relevant to the position and project responsibilities, staying abreast of industry advancements and best practices.
• Ad Hoc Activities: Perform other activities as requested by the project team or management.

Qualifications:

• Bachelor’s degree with a minimum of 3 years of pharmaceutical industry experience or an experienced Registered Nurse (R.N.) with clinical research exposure.
• Excellent written and oral communication skills.
• Proficiency in reviewing and interpreting clinical trial data and related documents.
• Strong organizational skills with the ability to manage project timelines effectively.

If this role sounds like it could be of interest, please apply now!