Site Relationship Coordinator

at  Medpace Inc

London EC4V, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate29 Jul, 2024Not Specified02 May, 20241 year(s) or aboveCommunication Skills,Medical Terminology,English,Trial Management,Drug DevelopmentNoNo
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Description:

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.

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


REQUIREMENT SUMMARY

Min:1.0Max:6.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

BSc

Health-related field

Proficient

1

London EC4V, United Kingdom