Are you ready to make a significant impact in the world of clinical data management? We are seeking a dedicated professional to support Clinical Data Management (CDM) delivery of high-quality data for assigned medium complex clinical studies. This role offers the opportunity to collaborate with DM vendors and liaise with various departments on a local and/or global level. If you are solution-oriented and can adhere to methodology standards, this could be the perfect role for you!

In this role, you will provide study level CDM administrative support based on the relevant model and DM Vendor. This includes activities related to the study start-up, conduct, and closeout phases. You will be responsible for study status reporting, collaboration with Data Management Vendor regarding upcoming deliverables, and oversight of the data quality. You will also be responsible for meeting Quality Compliance requirements, Trial Master File compliance for audit readiness, and performing User Acceptance Test of internal and external electronic Data Capture systems as required.

• University or college degree in the life sciences or related subject, pharmacy, nursing or equivalent relevant degree.

• Clinical Data Management Experience.

• Fluent English (oral and written)

• Attention to detail to ensure quality

• Good verbal and written skills

• Ability to work flexibly on simultaneous projects and proactively manage time to meet own deadlines.

• Strong interpersonal skills and proven ability to communicate effectively in a global environment.

Desirable Skills/Experience:

• Basic understanding of clinical trials methodology, GCP and medical terminology

• Understanding of database structures, programming languages, data standards (CDISC) and practices as they apply to CRF design, database development, data handling and reporting.

• Knowledge of SQL, 4GL, VBA or R software