Junior CRA
Warszawa
Junior CRA
Warszawa
Nr Ref.: 1021503
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
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
|
hays.pl |