Das ist der Job
EPM Scientific are currently partnered with a client running a global project in Aesthetic Medicine.
Darum lohnt es sich
They are urgently seeking a Freelance Clinical Research Associate to support their expanding clinical operations team.
See a short summary below: Contract Conditions Location: Germany, Remote Project: Medical Device, Aesthetic Medicine Key Responsibilities Conduct site monitoring visits (pre-study, initiation, routine, and close-out) to ensure compliance with protocol, GCP, and regulatory requirements.
Serve as the primary point of contact for investigator sites, ensuring high-quality data collection and patient safety. Support site selection, feasibility assessments, and start-up activities. Identify and resolve site-level issues, escalating risks as needed to ensure timely trial delivery.
Maintain accurate and timely documentation of monitoring activities and site communications. Contribute to continuous process improvement and best practices in clinical operations. Requirements Bachelor's or Master's degree in Life Sciences or related field preferred. Strong (5+ years of experience preferred) as a CRA.
Strong understanding of ICH GCP, and clinical trial processes. Experience in Aesthetic Medicine clinical trials is a must. Excellent organizational, communication, and interpersonal skills. Ability to work independently and manage multiple sites in Portugal. Willingness to travel up to 60%.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network. #J-18808-Ljbffr
