You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
Your ideas influence the way we work, and your voice matters here.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
Join us and build your future here.
What You'll Be Doing:
- Creates electronic Case Report Forms (eCRFs) according to finalized protocols and study design specifications for Electronic Data Capture (EDC) studies
- Creates data entry screens according to the approved annotated Case Report Form (CRF) for paper studies
- Communicate with data management and study management teams throughout all study start up activities to ensure team needs are understood and met.
- Designs, builds, and tests clinical databases according to Standard Operating Procedures (SOPs)
- Programs field derivations, edit checks, consistency checks, validations, procedures and rules.
- Develops of study reporting environment which includes CRF and non-CRF (loaded) data in addition to transforming collected data to required reporting format.
What We Are Searching For:
- Bachelor's degree, or international equivalent from an accredited institution, preferably in a technical field, or equivalent combination of education, training and experience
- 0 to 3 years of practical experience using commercial clinical data management systems and/or EDC products (eg - Oracle RDC / Inform, Medidata Rave, DataLabs, etc). Alternately, must have proven experience in all primary job functions.
- 1 to 2 years of SQL programming experience preferred
- Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverables, and task ownership
- Demonstrates excellent English verbal and written communication skills ·
- Familiarity with drug development and clinical trial processes preferred
We offer a comprehensive salary and benefits package, which includes health insurance (Doverie), 23 days of annual leave, food vouchers, additional payment for internet (all remote employees are eligible) and an Employee Assistance Program.
Additional details:
- Remote Position
- Fixed Term Contract – from September until the end of December 2026
- Working Hours – 11AM to 7PM, Monday-Friday
