Support the Lead DM as a back-up and team member, ensuring timely tasks
May perform data entry for paper-CRF studies, as needed
May perform quality control of data entry
May develop CRF specifications from the clinical study protocol and coordinate stakeholder feedback
May assist in building clinical databases
Conduct database build UAT and maintain quality controlled database build documentation

🎯 Requirements

Bachelor's degree and/or related experience
Around 2 years’ CDA experience in CRO/Pharma/Biotech
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
Able to handle a variety of clinical research tasks
Excellent organizational and communication skills
Professional written and spoken English

🎁 Benefits

Discretionary annual bonus
Private medical insurance
MultiSport Card
Life insurance
Pension
Home working allowance

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