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Hays Poland

Junior CRA

Warszawa, mazowieckie Full time

Hays Poland

Junior CRA

Warszawa
Junior CRA
Warszawa
NR REF.: 1021503

Junior Clinical Research Associate

Permanent, Fulltime Office based, Warsaw

An exciting opportunity has arisen for an experienced Junior CRA to work with an international Clinical Research Organisation that has a presence in Europe.

Key Duties and Responsibilities:

Identify and Manage trial sites; Conduct Site visits; Involvement in CRF development and review; Negotiation of site budgets; Clearly document all observations in writing in a timely manner following accepted business writing standards; Facilitate and assist in the response to company, client and regulatory audits

Key Requirements:
Life science/nursing graduate (or equivalent) plus relevant work experience; You will have up-to date training in ICH – GCP; Minimum of 6 months industry experience and must have co - monitoring experience at a minimum; Strong communication skills are a must, also experience of training team members and presentations skills will be desirable; Good understanding of the drug development process with emphasis on the clinical monitoring; Strong interpersonal and communication skills, both verbal and written; Excellent organisational skills and attention to detail; Able to work independently and as a team member; Able to prioritise, multi-task and meet deadlines


If this role is of interest please contact Marek Nadolnik at nadolnik@hays.pl
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Hays Poland

Job Description

Junior CRA
Warszawa
NR REF.: 1021503

Junior Clinical Research Associate

Permanent, Fulltime Office based, Warsaw

An exciting opportunity has arisen for an experienced Junior CRA to work with an international Clinical Research Organisation that has a presence in Europe.

Key Duties and Responsibilities:

Identify and Manage trial sites; Conduct Site visits; Involvement in CRF development and review; Negotiation of site budgets; Clearly document all observations in writing in a timely manner following accepted business writing standards; Facilitate and assist in the response to company, client and regulatory audits

Key Requirements:
Life science/nursing graduate (or equivalent) plus relevant work experience; You will have up-to date training in ICH – GCP; Minimum of 6 months industry experience and must have co - monitoring experience at a minimum; Strong communication skills are a must, also experience of training team members and presentations skills will be desirable; Good understanding of the drug development process with emphasis on the clinical monitoring; Strong interpersonal and communication skills, both verbal and written; Excellent organisational skills and attention to detail; Able to work independently and as a team member; Able to prioritise, multi-task and meet deadlines


If this role is of interest please contact Marek Nadolnik at nadolnik@hays.pl

Additional Information

Last updated
Employment type
Full time
Contract type
Permanent
Number of vacancies
1
Min. experience
One year
Min. education
Associate degree
Industry / category
Jobs in Laboratory / Pharmacy / Biotech