Overview
Do you have experience in creating data transfer agreements? Are you looking to work with new types of non- CRF electronic data, electronic data with complex data structures?
Responsibilities:
- Provides specialised expertise in the collection of electronic data (non- CRF data).
- Creates data transfer agreements for new types of data streams or data with complex structures and/or content.
- Supports the development of data transfer agreements for standardised data streams.
- Liaises with key stake holders to understand the data collection requirements.
- Liaises with the external vendors to ensure data delivered is of high quality and as per requirements.
- Performs quality control on test transfers to ensure data received is of high quality and the requirements are met.
- Collaborates with external vendor, Data Managers and Clinical Programmers to ensure the delivery of the raw data in to a SDTM format.
- Manage internal stakeholder expectations and drive delivery forward.
- Manage the resolution of issues and escalate accordingly to leadership team.
- Serve as a Subject Matter Expert for a given data stream.
- Lead/ participates in initiatives to improve processes.
About You:
- Bachelor’s degree in a technological or clinical field.
- 3+ years of relevant industry experience.
- Experience in creating data transfer agreements.
- Displays ability to interpret the data collection requirements from the clinical trial protocol
- Experience in working with non-CRF electronic data (Eg. Laboratory data, IWRS, ECG)
- Understands the requirements to transform non-CRF raw electronic data in to a SDTM format would be an advantage.
- Experience in having a client facing role.
- Exhibits excellent written and oral communication and excellent presentation skills.
- Comfortable with collecting, interpreting or explaining data or information to deliver messages to audiences not knowledgeable about the subject matter.
