Do you want to use your technical expertise to ensure data quality that contributes to the development of tomorrow's pharmaceuticals and medical devices?
We at CTC are now recruiting an eCRF Manager to our Biometrics department in Uppsala, where statisticians and statistical programmers also work. In this role, you will translate clinical study protocols into a high-quality eCRF, from planning and setup to validation, data review, and database lock.
The role involves many points of contact, both internally and externally. You work both independently and in close collaboration with colleagues in clinical study teams, primarily on:
Review relevant parts of study protocols and identify requirements, ambiguities, and needs related to eCRF and Data Management
Plan and configure eCRF and ePRO in EDC
Customize forms and program controls using JavaScript
Conducts and document validation, testing, and quality assurance
Manage eCRF permissions and support eCRF users, and contribute to relevant agreements and plans
Validate collected data during the study and take responsibility for database lock, delivery, and archiving
Coordinate work with relevant functions, follow up on decisions, and participate as an expert in eCRF and Data Management in, for example, client meetings
Contribute to the development of eCRF-related processes, standards, and SOPs.
Who we are looking for
We are looking for someone who works carefully, analytically, and systematically and values delivering optimal quality within agreed timeframes. You analyze protocols and technical problems methodically, ask clarifying questions, and follow up to ensure solutions work in practice. You drive your work forward independently, but you also recognize when an issue needs to be anchored or escalated.
Since the role has many points of contact, you need to be able to translate needs between different professions, be receptive to different perspectives, and collaborate in a solution-oriented manner. You treat colleagues, clients, and subcontractors with respect and professionalism and contribute to the team's common goals. We also value that you share CTC's values: Innovation, Community, Respect, Commitment, and Professionalism – iGREP.
Requirements:
Post-secondary education in computer science or another relevant field – alternatively equivalent technical knowledge acquired through work experience.
Good technical understanding and strong knowledge of JavaScript
Good ability to express yourself in Swedish and English, both orally and in writing.
Merits:
Experience with eCRF, ePRO, or Data Management in clinical trials
Experience with clinical trials or research and knowledge of Good Clinical Practice (GCP)
Experience with Viedoc or another EDC system
What we offer
At CTC, you have the opportunity to work close to the entire clinical study chain in a knowledge-intensive organization with short decision-making processes and a vibrant culture. We help each other, share knowledge, and leverage each other's strengths. With clear goals, trust, and shared commitment, we help new pharmaceuticals and medical devices reach patients.
We offer a collective agreement with associated insurance packages, as well as wellness contributions, wellness hours, and flexible working hours to help you balance your work and personal life. The position is located in Uppsala. During the introduction, you will work on-site; thereafter, hybrid work is possible up to two days per week based on the needs of the organization and projects.
Application
This is a permanent full-time position with a 6-month probationary period. Start as soon as agreed. Selection and interviews are ongoing, which means the position may be filled before the application deadline. Don't wait to submit your application.
If you have questions about the position, please feel free to contact the recruiting manager: Eva Jacobsson, 070-271 31 49, [email protected]
We look forward to learning more about you and what you can bring to our team!
This recruitment is handled entirely by CTC. We therefore ask that you refrain from contacting us from recruitment firms or advertising sales.