About the Role: We are seeking a detail-oriented Clinical Project Assistant to join a dynamic Study Build team at a leading global life sciences technology company. This is a fully remote position based in Denmark. The successful candidate will play a key role in translating complex clinical research protocols into electronic data capture system requirements, collaborating cross-functionally with internal teams and clients to ensure seamless study builds. Key Responsibilities:
Review clinical protocols and project documentation to define scope and requirements for study buildsAssist in designing and overseeing electronic Clinical Outcome Assessment (eCOA) system configurationsCollaborate with Study Operations Leads to identify resource needs and project timelinesDefine system requirements including form content, metadata, and regulatory compliance considerationsConduct internal User Acceptance Testing (UAT) and manage client UAT processesLead meetings internally and with clients to align on study design and system functionalityGenerate and update study-related reports and maintain standard design librariesCoordinate with project management, data management, and programming teams to ensure data export and mapping requirements are metSupport training initiatives and assist with change control scopingQualifications:
Bachelorâs degree in clinical trial design, life sciences, or equivalent experienceSolid understanding of clinical research processes, protocol design, and regulatory standardsStrong communication, organizational, and multitasking skillsProficiency in Microsoft Office (Word, Excel)Ability to work independently and quickly learn complex software and processesExperience in clinical research, electronic data capture, or related fields preferredPlease click âapplyâ or contact David Rowland (Recruiter II) at Planet Pharma for more information: E: Drowland@planet-pharma. co. ukT: +44 20 3928 8381About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field.
Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. www. planet-pharma. com
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