Associate Director, Study Start-Up

Medpace; München; Vor Ort; EUR 60.000 - 110.000; Vollzeit

Zusammenfassung

An established industry player is looking for a key manager to lead their Study Start-up group in Munich. This pivotal role involves strategic development, team management, and enhancing processes within clinical operations. You will engage with clients, oversee regulatory submissions, and drive continuous improvement initiatives. Join a dynamic organization that has made a significant impact in clinical research and is committed to advancing medical therapeutics. This is a fantastic opportunity for an experienced leader to make a difference in a supportive and innovative environment.

Leistungen

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifikationen

• 10+ years of leadership experience in Study Start-Up within a CRO or pharmaceutical company.
• Strong customer focus and ability to manage priorities in stressful situations.

Aufgaben

• Contribute to the growth and strategic development of the Study Start-Up team.
• Oversee regulatory submission activities and ensure compliance with protocols.

Kenntnisse

Presentation Skills

Negotiation Skills

Leadership Skills

Interpersonal Skills

Written Communication

Oral Communication

Customer Focus

Ausbildung

Bachelor's degree in life sciences

Advanced degree in a related field

Jobbeschreibung

Job Summary

We are seeking a key manager to support the Medpace Study Start-up group in Europe while being office-based in Munich. This position will be an integral part of the Medpace clinical operations management team. This role will be responsible for the strategic development of the group, management of the team, and continuous improvement of processes. As a leader of the Study Start-up team, you will be responsible for providing input on new business development opportunities and developing and maintaining relationships with clients. You will also be responsible for providing guidance and expertise to the Regulatory Submissions team in terms of competent authority and IRB/EC/REB submissions, as needed. Additional/alternative expertise in other facets of Study Start-up are welcome.

Responsibilities

• Contribute directly to the 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 to ensure they are in accordance with Medpace standard operating procedures and study protocols;
• Provide input on new business development opportunities;
• Develop and maintain relationships with clients; and
• Support the local German team development.

Qualifications

• Bachelor's degree in life sciences or a related field - an advanced degree is 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; and
• Experience managing and developing a team.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets