MISSION

FutureMeds is an independent, fully owned European Site Network and DCT service dedicated to conducting high-quality clinical trials for Sponsors & CROs.
With a strategic focus on patient experience, we are driven by the purpose of helping bring quicker access to life-changing medications and therapies to all those who need them through connecting a global healthcare community.

Guided by the Progress P.A.C.T. (People, Access, Collaboration, Truth), our company promise to our patients, partners & team, we foster a culture that enables us to drive progress:

• Our Patients benefit from progress to their health & care.
• Our Partners benefit from progress to their research projects, helping them increase their impact on worldwide healthcare.
• Our Team benefit from progress to personal & professional growth.

We’re looking for an ambitious and dynamic Junior Feasibility & Proposal Specialist to join our global Commercial team. The role will act as a support in managing clients request for information and proposals including feasibility questionnaires completion.
Based from our core locations in Germany with travel to other European locations as required, you will report to the Manager of Feasibility, in providing support on feasibility and proposals development, preparing necessary metrics, completion of feasibility questionnaire, aiding in clients communication by monitoring progress of completed feasibilities with clients such as Sponsors, Contract Research Organizations (CROs), and BioTech companies; ensuring that all studies are being follow up and collaborate closely with the commercial team to further close all open proposals.
This is an exceptional opportunity for a dynamic and ambitious developing professional to work at the heart of clinical trial agreements and accelerate their career in a fast-growing market disrupting company

• Reviewing RFIs/RFPs: Reviewing clients/internal team requests to ensure delivery of proper information.
• Feasibility completion: working with the team to develop the accurate responses representing the site network’s potential
• Developing proposals: Working with internal teams to best address the individual client’s needs.
• Ensuring Compliance: Making sure all data are correct and reflect the current knowledge.
• Protocol analysis: mapping the study protocol activities with current site capabilities and medical resources
• Risk Management: Identifying potential risks in study execution terms and proposing mitigation strategies.
• Maintaining Records: Keeping detailed records of all feasibility/proposals-related documents and communications.
• Coordinating with Stakeholders: Collaborating with commercial, medical, finance, and operations, for input.
• Study closure: monitoring the timely communication under feasibility angle to make sure all proposed sites are being followed up on the outcome status.