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Senior/Clinical Site manager II
Proclinical is recruiting on behalf of a client in Stockholm
A leading multinational contract research organisation, providing consultation in the biopharmaceutical and medical device sector, have a vacancy for a Senior/Clinical Site manager to be home-based in Stockholm, Sweden with the requirement to travel to client offices. The company employ over 15,000 personnel in over 50 countries.
Job Responsibilities:
- Act as the company's direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues.
- Build relationships with investigators and site staff.
- Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements.
CRA II/Senior CRA (oncology experience)
Covance is recruiting on behalf of a client in Stockholm
We are currently looking for talented Clinical Research Associates (3 vacancies opened!) to work for us in the Co-source Department as our sponsor, a well-known pharma company, is currently expanding their Clinical Operations team. These are full-time, permanent and home-based positions in Sweden.
Responsibilities include:
- All aspects of site management as prescribed in the project plans
- Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
- Negotiation of study budgets with potential investigators and collaboration with Covance Legal Department with statements of agreements
Senior Country Submission Specialist
Syneos Health is recruiting on behalf of client in Stockholm
We are currently looking to strengthen our Ethics and Regulatory department in the Nordics and are seeking an experienced SSU & Regulatory Specialist with Site Contracts experience to be based in either Sweden or Denmark.
A brief summary of duties you will be involved in as a Site Startup Specialist
- Reviewing essential document packages for site activation
- Preparation and submitting of Central EC Applications, Local EC Applications, - RA Applications, and other local regulatory authorities or hospital approval submissions as required
- Reviewing Informed Consent Forms
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