Digital Biomarker Associate (Pharma/Medical Device)
Posted on Apr 22, 2020 by NextLink Solutions
Are you looking for an interesting and challenging opportunity in Switzerland?
NextLink is looking for a Digital Biomarker Study Associate (Pharmaceutical/Medical Device) to work in Basel, Switzerland for a 12 month contract (possible extension) for a multinational client.
NextLink Solution, a Swiss IT Consultancy Company that has been providing both IT services and IT staffing to major customers for the past 20 years, has an excellent opportunity that can take your career to the next level.
Job Title: Digital Biomarker Study Associate
Start date: ASAP
End date: 12 months (possible extension)
Location: Basel, Switzerland
Remote/Home Office: up to a day per week after onboarding and strong performance
Must Have Skills:
Minimum 3 years' experience in clinical operations in either pharma or medical devices*
Strong experience with vendor management*
Very good university degree (BA. level or above) in Sciences or related fields*
Passion for digital innovation in healthcare, and especially for leveraging novel technologies to modernize clinical endpoints and improve disease/treatment management
Excellent analytical skills
Excellent communication and presentation skills
Self-starting team player
Problem solving attitude and structured approach to work
Native/fluent English or equivalent
Nice to have skills:
Previous experience working for/with an eCOA (electronic clinical outcome assessment) vendor*
Tasks & Responsibilities:
Provide operational support for remote patient monitoring solutions in studies, including by being a point of contact for support requests by physicians and study coordinators
Develop translation, logistics, support and related processes, and select/manage vendors that provide these services
Ensure support requests are promptly addressed by the digital biomarker team
Preparation of site supporting materials, including training materials
Assist with preparing remote patient monitoring parts of IRB/Ethics Committee submissions, and addressing follow up questions
Create and maintain accurate study level progress information (eg recruitment status, remote patient monitoring data generation levels, data transfer status, technical issue overviews) through the efficient use of systems, tools and reports.
Create and maintain centralized project/team work-spaces, including document creation and/or maintenance.
Assist with effective communication and information sharing via compilation of study-specific documents and resources (agendas & minutes, presentations, team contact lists, distribution lists and other relevant material).
Identify and contribute to areas of best practice and process improvements.
Proficiency with MS Office suites such as Excel, PowerPoint, Word