Site Relationship Coordinator
at Medpace Inc
London EC4V 3BJ, , United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | 1 year(s) or above | Drug Development,Medical Terminology,Communication Skills,English,Trial Management | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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 3BJ, United Kingdom