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Clinical Research Associate (CRA)
SOCAR Research —Nyon, VD
- Doktorat
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- Tagschicht
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- Englisch
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Edwards Lifesciences —Nyon, VD
- 100%
- Microsoft Excel
- Management-Erfahrung
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- Microsoft Powerpoint
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Senior Clinical Safety Specialist (EU Remote)
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- 100%
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Sr. Director, Compound Operational Lead (m/f)
Merck Group —Eysins, VD
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- Bachelor
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Clinical Research Associate (CRA)

SOCAR Research
Nyon, VD

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Details zur Stelle

Qualifikationen

Französisch
Doktorat
Englisch
Microsoft Office
Klinische Erfahrung
Master
Bachelor
PC-Kenntnisse
Italienisch
Kommunikationsfähigkeit
Deutsch

Vollständige Stellenbeschreibung

SOCAR Research, located in Nyon, Switzerland, is a leading Functional Service Provider with more than 30 years’ experience in the provision of clinical research and technology services to the pharmaceutical, biotechnology and medical device industries. SOCAR is seeking to hire an experienced Clinical Research Associate (CRA). You will be part of a young and dynamic multidisciplinary project research team. Part of your responsibilities will be to perform clinical monitoring (remote and onsite) for designated projects and the remainder of the time will be office-based and will be spent, amongst others, performing tasks in data management such as checking clinical data for completeness and medical consistency, in preparation for statistical analysis.

Your responsibilities will include:

Perform (remote) site visits, write-up the visit reports, follow-up and resolve issues arising from these visits

Perform source data/document verification (SDV) remotely and onsite

Perform (remote) source data review

Perform remote monitoring / site management activities

Maintain the electronic Trial Master File (eTMF)

Perform data management activities (e.g. tracking the completion of the eCRFs at the site and perform data cleaning activities)

Limited travel to sites

Your Profile:

Medical-related scientific degree (Bachelor, Master, PhD, Nursing qualifications or similar degrees and/or experience)

A minimal of three years’ experience as a Clinical Research Associate (CRA)

Strong working knowledge and understanding of ICH-GCP, Swiss and other international laws and regulations governing clinical trials

Strong medical/clinical knowledge

Excellent clinical trial monitoring skills with a high level of attention to detail and sound problem solving skills

Excellent interpersonal communication skills (verbal and written)

Ability to prioritise multiple tasks and achieve project timelines

Computer skills (MS Office) and experience in eCRF systems, CTMS Systems, as well as eTMF Software

Fluent English and German (written and spoken); French and Italian is a plus

Show commitment to and perform consistently high quality work

If you possess a valid Swiss work permit and fit the profile required for this versatile and challenging position, please forward your application to [email protected] - we look forward to talking to you. We will only respond to candidates who fit the profile for this position.

SOCAR is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law.

Only direct applications will be considered for this vacancy. We do not accept speculative CVs or candidate profiles.

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Erweiterte Suche

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