CRA (Level I) FSP - Athens

Position Overview

• Location Type: Onsite
• Employment Type: Full Time
• Work Schedule: Standard (Mon-Fri)
• Salary: Not specified
• Job Description: At PPD, part of Thermo Fisher Scientific, you can have meaningful work that has a positive impact worldwide. Join us in bringing our Mission to life - helping customers create a healthier, cleaner, and safer world. We support our teams in achieving their career goals while advancing science through research, development, and delivery of life-changing therapies. Our work includes clinical trials in 100+ countries and innovative approaches to clinical research in our PPD clinical research portfolio. We cover laboratory, digital, and decentralized clinical trial services. By delivering quality and accuracy, you will contribute to better health outcomes for people and communities. This is a great opportunity for CRA's currently working within the life science sector to work with a world-leading CRO and dedicated to one of our Clients.

Requirements

• University degree or equivalent experience in a science-related field
• Understanding of ICH-GCP, EU, and FDA requirements
• Proficiency in English
• 2 years’ experience in Interventional studies
• Knowledge of medical/therapeutic area knowledge and medical terminology

Responsibilities

• Applies root cause analysis (RCA), critical thinking, and problem-solving skills to identify site processes failure and take corrective/preventive actions to ensure compliance and reduce risks.
• Ensures data accuracy through SDR, SDV, and CRF review as applicable through on-site and remote monitoring activities.
• Assesses investigational product through physical inventory and records review.
• Details observations in reports and letters according to timelines using approved business writing standards.
• Advances observed deficiencies and issues to clinical management expeditiously and follows all issues through to resolution.
• Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution.
• Participates in investigator meetings as necessary.
• Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted.
• Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations.

Skills, Knowledge, and Abilities

• Proven clinical monitoring skills
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations, and procedural documents
• Well-developed critical thinking skills
• Good oral and written communication skills
• Ability to maintain customer focus through the utilization of good listening skills and attention to detail
• Good organizational and time management skills
• Effective interpersonal skills
• Attention to detail
• Ability to remain flexible and adaptable in a wide range of scenarios

Travel

• Traveling (Not specified - assumed to be required)

Working Conditions

• Office environment

Schedule

• Monday-Friday 09:00-17:00