Clinical Research Associate/Code: ClinRA - HeaDS
Τετάρτη 11 Ιούλ 2018

Health Data Specialists (HeaDS), an Athens based CRO with a global reach, is seeking a CRA for its international Clinical Trials program.

The CRA role will be based in Athens and be involved in interventional Clinical Trials across multiple Therapeutic Areas with key focus on Oncology/Hematology.

Job Description:

  • Participate in the site selection process.
  • Execute operations on new and on-going clinical research projects to ensure successful project deliverables.
  • Perform all site monitoring visit activities, inclusive of all study visit types, as per protocol requirements and serve as the principal point of contact for investigational sites.
  • Manage timely subject enrolment and quality data collection.
  • Ensure patient safety is maintained and informed consent procedures are carried out.
  • Prepare and update the Clinical Trial Files, ensuring the proper collection of essential documents.
  • Verify the receipt, handling, accounting, storage conditions and availability of clinical products.
  • Liaise with vendors such as central laboratories as required to ensure protocol adherence and ensure investigational sites have appropriate clinical supplies.
  • Perform / assist in regulatory submissions.
  • Establish updates, track and maintain study specific trial management tools/systems, and status reports as required.
  • Communicate effectively with team members and management to relay protocol/study issues and implement necessary actions in response to those issues.
  • Assess adherence to SOPs, GCP and all applicable regulatory requirements.

Job Requirements:

  • Bachelor’s and/or master’s degree (preferred in Health Sciences)
  • Previous Work Experience:
  • Minimum 2 years’ work experience as a CRA in either interventional trails or NIS
  • Knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial management
  • Very strong written and verbal communication skills in both Greek and English
  • High organizational and logistical skills to ensure effective management of multiple sites and protocols within timeframes.
  • Strong ability to build and maintain relationship with investigators, member sites and with pharma/biotech companies for business relations.
  • MS Office (Excel, Word, Power Point).
  • Ability to travel

Join us to be part of a multidisciplinary team of highly skilled scientists in the forefront of Clinical Research within a friendly work environment. Competitive remuneration package comes on top.

Please submit your application via email to info@heads.gr indicating the position code.
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