Back to search.SEC Recruitment Ltd - CLINICAL RESEARCH ASSOCIATE - LISBON
| Employment Type: | Permanent |
| Location: | Lisboa - Grande Lisboa, Portugal |
| Salary: | |
| Languages: | English, Portuguese |
Responsibilities include: Perform site selection, initiation, monitoring and close-out visits. Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. May provide assistance to less experienced clinical staff.
Successful candidates will hold a Degree, in a scientific or healthcare discipline, advanced level of English, complimented all by solid prior monitoring experience.
A competitive salary is on offer and this is an urgent requirement so for immediate consideration and a full job description on a request please forward your CV to beatriz.deluis@secpharma.com or call + 44 (0) 207 255 6600
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. May provide assistance to less experienced clinical staff.
Successful candidates will hold a Degree, in a scientific or healthcare discipline, advanced level of English, complimented all by solid prior monitoring experience.
A competitive salary is on offer and this is an urgent requirement so for immediate consideration and a full job description on a request please forward your CV to beatriz.deluis@secpharma.com or call + 44 (0) 207 255 6600
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