Clinical Oversight Manager
vor 1 Woche
Proclinical have partnered with a mid-sized Biotech focussed within Rare Diseases who are recruiting for a Clinical Oversight Manager. They have had several successful product launches over last few years and are presently running multiple phase III trials within highly multifaceted therapy areas. You will be responsible overseeing several studies within one program. You will be responsible for overseeing the CRAs of the CRO, lead site activation across Europe and be involved in developing patient recruitment strategies.
This is a great opportunity to move into a truly international role and to join a company with numerous programs continuing. This is an initial 12 month contract with flexibility to work from home. This position requires professional working proficiency in French.
**Skills & Requirements**:
- At least 5+ years of experience in a clinical study management role within a Pharma or Biotech organisation.
- Familiarity in vendor management.
- A CRA background and experience in co-monitoring would be ideal.
- Prior involvement in highly multifaceted therapy areas would be preferable.
- Exhibited multitasking, project management and implementation abilities.
- Interpersonal, presentation, persuasion, influencing and communication skills both verbally and in writing.
- An organised individual who is efficient, punctual and collaborative within a team setting.
- Computer literacy in MS Office.
Proclinical Staffing is an equal opportunity employer.
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