Site Relationship Coordinator
London | careers.medpace.com |
Job Summary :
Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team in London. 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 the UK.
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 :
• Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;
• Develop effective plans for site contact and follow-up;
• Support management in expediting feasibility, site selection and study start-up; and
• May be responsible for other projects and responsibilities as assigned.
Qualifications :
• Minimum a Bachelor of Science in health-related field;
• Minimum 1 years' site and clinical trials experience (more experience for the more senior positions required);
• CRA experience is an asset;
• Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred;
• Knowledge of medical terminology and clinical patient management preferred;
• Fluency in English;
• Demonstrated organizational and prioritization skills;
• Excellent oral and written communication skills; and
• 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. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.
WHAT TO EXPECT NEXT
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an initial phone interview.
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? :
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Perks:
• Flexible work hours
• WFH opportunities
• Career development
• Annual salary review
• Working environment: join a motivated team in our new offices based near Lyon Part-Dieu station.
Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team in London. 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 the UK.
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 :
• Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments;
• Develop effective plans for site contact and follow-up;
• Support management in expediting feasibility, site selection and study start-up; and
• May be responsible for other projects and responsibilities as assigned.
Qualifications :
• Minimum a Bachelor of Science in health-related field;
• Minimum 1 years' site and clinical trials experience (more experience for the more senior positions required);
• CRA experience is an asset;
• Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred;
• Knowledge of medical terminology and clinical patient management preferred;
• Fluency in English;
• Demonstrated organizational and prioritization skills;
• Excellent oral and written communication skills; and
• 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. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.
WHAT TO EXPECT NEXT
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an initial phone interview.
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? :
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Perks:
• Flexible work hours
• WFH opportunities
• Career development
• Annual salary review
• Working environment: join a motivated team in our new offices based near Lyon Part-Dieu station.
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