senior cra – ψυχικο

Are you at least 3 years experienced Clinical Research Associate (CRA or Senior CRA)? Are you looking for your next step development in the Clinical Research Associate (CRA or Senior CRA) career path? Do you wish to experience innovation in your next career step as a Clinical Research Associate (CRA)?

If you are ready to make your next career step as Clinical Research Associate (CRA or Senior CRA), we are keen to speak with you today!!! Read below and apply now!

benefits

Some of the advantages you can expect from your role a Clinical Research Associate (CRA) are:

• A competitive compensation package is provided
• Consistent workload
• Career development opportunities 

responsibilities

The Clinical Research Associate (CRA or Senior CRA) will perform monitoring and site management activities for Phase II-IV clinical research projects to assess the progress of clinical projects and to ensure they are conducted, recorded, and reported in accordance with the protocol, Company and Sponsor standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Primary Responsibilities

• Performing site selection, initiation, monitoring and close-out visits (on-site or remotely), according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
• Evaluating the quality and integrity of site practices
• Supporting the development of a patient recruitment, retention and awareness plan
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• Preparation and attendance of Investigator Meetings
• Act as a primary liaison with Sponsor and study site personnel

requirements

The following qualifications will make you the ideal candidate for the CRA or Senior CRA role:

• University degree in life sciences, pharmacology, biology or chemistry
• At least 3 years of previous demonstrated experience in the clinical field, including a minimum of 2 year experience in clinical monitoring of Interventional Clinical Studies (pre-study, initiation, routine monitoring and closeout visits).
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Excellent command (written and verbal) of English language and proficient knowledge of medical terminology
• IT literacy (MS Windows, MS Office, Internet Use)
• Solid understanding of the drug development process and pharmaceutical legislation
• Excellent organizational, prioritizing and communication skills
• Ability to manage multiple and varied tasks with attention to detail
• Effective time management to ensure project deadlines are met
• Ability to manage required travel of up to 40% on a regular basis

information

If this sounds like you, we want to hear from you today!

For further info please contact Dora Tzevelekou

Please note that for transparency and equity reasons, only those applications made online via our site will be assessed. After the screening of all the CVs received, we will only contact the candidates who meet the requirements of the job to arrange an interview. ​ All applications are considered strictly confidential.