Clinical Trial Site Relationship Coordinator

Medpace, Inc.; Deutschland; Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

Join a vibrant Clinical Operations team as a Clinical Trial Site Relationship Coordinator in Munich. This role offers a unique opportunity to engage with clinical research, focusing on building strategic relationships and conducting feasibility assessments. You will be instrumental in supporting site operations and ensuring quality study delivery while working within a company recognized for its innovative approach to drug development. If you are looking for a challenging yet rewarding career in a supportive environment that values professional growth, this position is perfect for you.

Leistungen

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifikationen

• 1+ year of clinical trials experience required, CRA experience is an asset.
• Knowledge of GCP guidelines and clinical trial management preferred.

Aufgaben

• Support sites with feasibility assessments and business opportunities.
• Build and maintain relationships with site networks and directors.
• Conduct regular performance reviews for participating sites.

Kenntnisse

Organizational Skills

Communication Skills

Clinical Trials Knowledge

Drug Development Knowledge

Microsoft Office Proficiency

Ausbildung

Bachelor of Science in health-related field

Jobbeschreibung

Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in Germany. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel.

If you want an exciting career within a company that excels in delivering innovative research and development of cutting-edge drugs, where you can grow your potential, then this is the opportunity for you.

Responsibilities

1. Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;
2. Develop effective plans for site contact and follow-up;
3. Support management in expediting feasibility, site selection and study start-up;
4. Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country;
5. Conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up;
6. Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention;
7. Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors;
8. Conducting regular performance reviews for sites participating in our studies, ensuring quality study delivery;
9. Serve as an escalation point for site related issues throughout the life cycle of a study;
10. Develop an intelligence database with site and country intelligence;
11. Support Management with process improvement initiatives regarding feasibility activities;
12. Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information;
13. May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.

Qualifications

1. Minimum a Bachelor of Science in health-related field;
2. Minimum 1 year of site and clinical trials experience (more experience for the more senior positions required);
3. CRA experience is an asset;
4. Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred;
5. Knowledge of medical terminology and clinical patient management preferred;
6. Fluency in English; German;
7. Demonstrated organizational and prioritization skills;
8. Excellent oral and written communication skills;
9. Proficient knowledge of Microsoft Office applications.

We kindly ask to send applications in English.

WHY MEDPACE?

At Medpace, you will find work that is both challenging and rewarding. You will be given the tools and training to succeed. You will be rewarded for strong performance and provided opportunities to grow professionally.

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.

Medpace Perks

1. Flexible work environment;
2. Competitive compensation and benefits package;
3. Competitive PTO packages;
4. Structured career paths with opportunities for professional growth;
5. Company-sponsored employee appreciation events;
6. Employee health and wellness initiatives.

Awards

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

EO/AA Employer M/F/Disability/Vets