Global Feasibility Strategist – Clinical Trials

Medpace; Greater London; Hybrid; GBP 40,000 - 60,000; Full time

Job summary

Medpace is seeking a Feasibility Coordinator to join our global clinical operations team. You will work cross-functionally with clinical operations, medical and regulatory submissions teams, researching databases, and gathering feedback from investigative sites to inform country selection and enrolment planning.

Responsibilities include coordinating feasibility assessments, proposing site and country strategies, outreaching to investigative sites, presenting results, and supporting bid defense

Qualifications

• PhD in life-sciences or 2 years CRO experience preferred.
• Analytical thinker with great attention to detail.
• Ability to prioritize multiple projects and tasks within tight timelines.
• Excellent written and verbal communication skills.
• Fluency in English language.
• Some clinical research experience is beneficial; and
• Working knowledge of feasibility processes and databases is highly desirable.

Responsibilities

• Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams
• Develop preliminary proposal strategy for site and country selection
• Perform outreach to investigative sites to obtain indication and protocol specific feedback
• Present feasibility results to members of the proposal team to assure correct assumptions were applied and strategy is in line with our therapeutic and operational experience
• Assist project teams with preparation for bid defense meetings; and
• Support departmental process improvement initiatives and general departmental administrative functions

Skills

Analytical thinking

Attention to detail

Prioritization

Communication

English fluency

Clinical research

Feasibility knowledge

Education

PhD in life-sciences

2 years CRO experience

Job description

Medpace is seeking a Feasibility Coordinator to join our global clinical operations team. You will work cross-functionally with clinical operations, medical and regulatory submissions teams, researching databases, and gathering feedback from investigative sites to inform country selection and enrolment planning.

Responsibilities include coordinating feasibility assessments, proposing site and country strategies, outreaching to investigative sites, presenting results, and supporting bid defense