Site Relationship Coordinator
We are seeking a full-time
Site Relationship Coordinator
to join our 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 suit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel. 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; May be responsible for other projects and responsibilities as assigned. Requirements:
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; Proficient knowledge of Microsoft Office applications. About 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.
We are seeking a full-time
Site Relationship Coordinator
to join our 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 suit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel. 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; May be responsible for other projects and responsibilities as assigned. Requirements:
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; Proficient knowledge of Microsoft Office applications. About 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.
