London-Based Study Start-Up Director

Medpace

Greater London

On-site

GBP 110,000 - 140,000

Full time

5 days ago
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Benefits offered by this job

Competitive compensation
Comprehensive health benefits
On-site London office
Ongoing training & development

Job summary

Medpace is seeking a key manager to lead the Study Start-Up group in Europe from our London office. You will drive strategic development, manage the team, and continuously improve processes within a global CRO environment.

You will guide Regulatory Submissions and support new business development, while fostering strong client relationships and leadership across the UK team. You will oversee timelines, ensure adherence to SOPs, and contribute to the growth of a high-performing Study Start-Up

Qualifications

  • Bachelor's degree in life sciences or related field; advanced degree preferred.
  • +10 years of Study Start-Up leadership experience within a CRO or pharmaceutical company.
  • Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills.
  • Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations.
  • Excellent written and oral communication skills; experience managing and developing a team.

Responsibilities

  • Contribute to growth and strategic development of a large, global Study Start-Up team.
  • Develop and identify continuous improvement opportunities of internal processes.
  • Oversee Study Start-Up/Regulatory Submission activities and timelines in line with SOPs and study protocols.
  • Provide input on new business development opportunities.
  • Develop and maintain relationships with clients; support the local UK team development.

Skills

Leadership
Presentation
Negotiation
Communication
Team leadership

Education

Bachelor's degree in Life Sciences

Job description

Medpace is seeking a key manager to lead the Study Start-Up group in Europe from our London office. You will drive strategic development, manage the team, and continuously improve processes within a global CRO environment.

You will guide Regulatory Submissions and support new business development, while fostering strong client relationships and leadership across the UK team. You will oversee timelines, ensure adherence to SOPs, and contribute to the growth of a high-performing Study Start-Up

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