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
RepresentErgomed at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies and for committee meetings, (e.g.EC/IRB)
Developreviewand editof 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 neuroscience, oncology, rare disease trials or complex studies
Experience in selecting and managing external service providers
Strong analytical, organisational, communication and numeracy skills
Minimum 5 years’ experience in CRO Industry.
Bachelors Degree in a science related discipline.
Additional Information
Why Should You Apply?
You want be involved in a wide range of interesting projects and studies
You'd likeyour achievements and hard work to be recognized
You want to work for a growing company where there are opportunities for advancement
You'd like to work in a company that has a great reputation with its clients and employees.
Making a difference to people's lives matters to you
