crc - psychiko

Δημοσίευση
Επικοινωνία
Ντόρα Τζεβελέκου, Randstad Hellas
Τύπος εργασίας
μόνιμη
Κάντε την αίτηση σας τώρα!

Περισσότερες πληροφορίες για αυτή τη θέση εργασίας

Δημοσίευση
Τοποθεσία
psychiko, αττική
Κλάδος
επιστήμες υγείας
Τύπος εργασίας
μόνιμη
Κωδικός θέσης εργασίας:
28934
Επικοινωνία
Ντόρα Τζεβελέκου, Randstad Hellas
Τηλέφωνο
2166001387

περιγραφή εργασίας

We are looking for an experienced CRC (clinical study coordinator). If you're dedicated and ambitious, the role of CRC is an excellent place to grow your career. 

Do you have at least 2 years of experience in clinical research field? Then don't hesitate to apply for the role of CRC.

Whatever your career goals, we are here to help you build a smart and flexible career with no limits! Read below and apply now!!! 

παροχές

Some of the advantages you can expect from your role as a CRC are:

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

αρμοδιότητες

As a CRC, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.

Primary Responsibilities

  • Participation in training.
  • Familiarization and compliance with studies core documents (e.g. protocol), processes and timelines.
  • Work with the Principal Investigator (PI) to develop and implement recruitment strategies in accordance with the study requirements.
  • Assist PI in assuring that all site investigational team members have met training requirements in accordance with the protocol, policies and procedures.
  • Maintain effective and ongoing communication with the sponsor, the PI and the site’s investigational team during the course of the study.
  • Pre-screen study subjects for eligibility, as instructed by the study protocol, coordinates subjects assessments and other study evaluations (e.g. central laboratories documentation and processes).
  • Assure timely completion of subjects (e)CRFs.
  • Assist investigational sites with IRB/IEC submissions and ensures collection of required essential documents for study start-up, regulatory submissions as well as throughout the conduct of the study.
  • Maintain adequate inventory of study supplies (medication and non-drug supplies). If handling investigational drugs/devices, follows the sponsor protocol and investigational drug accountability.
  • Maintain study files and records in accordance with sponsor requirements.

προσόντα

The following qualifications will make you the ideal candidate for the CRC role:

  • Bachelor’s degree in a related field or equivalent combination of education, training and experience.
  • Previous experience in Clinical Trials field gained from a Pharma or CRO is an advantage 
  • Computer proficiency, including Microsoft Office applications
  • Strong oral and written communication skills

δεξιότητες

  • Ethical work practice
  • Excellent research skills
  • Attention to detail
  • Critical thinking skills
  • Knowledge of budgeting and financial principals

εμπειρία

Required experience:

  • 1-2 years’ experience coordinating clinical research preferred

απαιτούμενη εκπαίδευση

  • Bachelor

πληροφορίες

If this sounds like you, we want to hear from you today! Should you need additional information, 

please contact me Dora Tzevelekou at 2166001387.

Please note that 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.