Clinical Research Associate II
Clinical Research Associate II - Sponsor dedicated
Location: Bucharest, Romania
Proclinical is seeking multiple CRAs to join a reputable CRO on a temporary basis n Romania. As a Clinical Research Associate II at our client, the successful candidates will work within a
- scale,
- paced environment alongside a
- knit team of highly qualified CRAs to identify, select, initiate and
- out investigational sites for clinical studies in phases I - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
For this position, our client is requesting to work office based 2 -3 days a week in Bucharest. This will enable the successful candidate to work closely with a dynamic and close knitted team in order to grow and learn quickly as a CRA. Being flexible to work in the office is essential for this opportunity.
Responsibilities will include:
- out visits for all sites.
Key Skills and Requirements:
- site monitoring experience
- solving skills
For more information, please apply.
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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Clinical Research Associate II - Sponsor dedicated
Location: Bucharest, Romania
Proclinical is seeking multiple CRAs to join a reputable CRO on a temporary basis n Romania. As a Clinical Research Associate II at our client, the successful candidates will work within a
- scale,
- paced environment alongside a
- knit team of highly qualified CRAs to identify, select, initiate and
- out investigational sites for clinical studies in phases I - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
For this position, our client is requesting to work office based 2 -3 days a week in Bucharest. This will enable the successful candidate to work closely with a dynamic and close knitted team in order to grow and learn quickly as a CRA. Being flexible to work in the office is essential for this opportunity.
Responsibilities will include:
- Complete selection, opening, tracking and
- out visits for all sites. - Supporting the development of a subject recruitment plan
- Assess the quality and integrity of site practices in accordance with regulatory requirements,
- Manage progress by tracking regulatory submissions, recruitment, case report form completion and data query resolution
- Collaborating with experts at study sites and with client representatives
Key Skills and Requirements:
- University degree in scientific discipline or health care
- Proven
- site monitoring experience - Good knowledge of clinical research regulatory requirements
- Very good computer skills including MS Office
- Excellent command of Romanian and English language.
- Strong organisational, time management and
- solving skills - Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Flexibility to travel
- Driver's license, class B
For more information, please apply.
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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