CRAII/Senior CRA job in Stockholm

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Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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This vacancy has now expired. Please see similar roles below...

An international research organization is seeking to recruit a Senior CRA to their office in Sweden. This Contract Research Organization (CRO) provides a broad range of product development and data solution services to pharmaceutical and biotechnology companies around the world. Based in Paris, this position is an exciting opportunity to work with an award-winning and globally renowned CRO.

Working as an integral part of the PRA full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle.

Job Responsibilities:

Taking full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.
Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

Skills and Requirements:

Educated to degree level in a life science discipline or be a licensed healthcare professional.
Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
Experience working on Oncology trials or complex studies would be an advantage for this role.
Study start up experience (Feasibility, Contract Negotiation, submissions) preferred.
Fluent in English and Swedish languages.
Demonstrable multitasking, project management, and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Sofia Amark at +442038618210 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

#LI-SA1

#ClinicalResearch

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