Job description
- Ensure the projects are delivered on time, within budget, and agreed scope, maintaining the appropriate industry, sponsor and Ergomed quality standards
- Liaise with project team members, provide training where needed and ensure correct allocation to tasks
- Develop, review and edit of project plans to assure consistency with project goals
- Organisation and facilitation of project meetings related to study activities (study organization, initiation, execution, closure)
- Point of contact with Sponsor and Ergomed Senior Management on project status
- Represent Ergomed at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies and for committee meetings, (e.g.EC/IRB)
- Develop review and edit of relevant SOPs to assure consistency with Regulatory standards and develop study related training programs to support this.
- Contribute to bid defence activities
Qualifications
- Experience of managing international clinical trials in a CRO environment
- Ideally knowledge of oncology, rare disease trials and / or complex studies
- Experience in selecting and managing external service providers
- Strong analytical, organisational, communication and numeracy skills
- Experience in CRO Industry
- Bachelor’s degree in a science related discipline.
PrimeVigilance d.o.o.
- Đorđa Stanojevića 14, Beograd, Srbija
- PIB: 109436311
- Matični broj: 21181986