Clinical Research Associate

Salary: £45000 to £999999
Contact name: Selina Maini

Contact email: selina.maini@medella.life
Job ref: 325
Published: about 2 months ago

The Company

My client is a European clinical CRO providing premium support for the management of global clinical trials from phase I to IV as well as pre- and post-marketing medical device investigations.

Founded in 1998, the company has 20 years of extensive experience in a wide range of therapeutic areas. Its recent oncology/immuno-oncology portfolio amounts to over 400 trials.

Their strength lies in its people and its specialized teams who assist clients from A-Z with medical writing, scientific and statistical consultancy for trial design and skilled teams of operational staff across Europe that ensure high quality project execution.

Position

We offer a great opportunity as Clinical Research Associate / Clinical Monitor for those who have a scientific background, enjoy travelling and are passionate about research.

Responsibilities

  • Collecting the documents required for the ethical and administrative submission

  • Checking the willingness to cooperate and the resources of the Investigator

  • Verifying the suitability of the site

  • Ensuring training and compliance with the protocol

  • Checking drug accountability and drugs delivery timeliness

  • Contacting sites to check the patient status, push enrollment and manage queries in a

    timely manner

  • Ensuring the correct completion of informed consent

  • Checking adherence to inclusion/exclusion criteria

  • Checking that the enrollment schedule is in line with the study plan

  • Managing CRFs and internal reporting

  • Checking the completeness and consistency of collected data

  • Verifying that serious adverse events are reported according to the company/Sponsor procedures

  • Handle study materials, including study drug(s), as foreseen for the specific study and as applicable

  • Promptly managing and follow-up protocol deviations

  • Participating in periodic meetings with Sponsors and Investigators

  • Maintaining a proactive relationship with the Data Center

Requirements

  • Master's Degree in scientific/healthcare related subject

  • CRA certification (for Italian candidates)

  • Willingness to travel

  • Good knowledge of English

  • Good planning, organization and problem-solving abilities

• Good communication and interpersonal skills


Connect

If you believe that you are the right person for this role, please apply now. Alternatively, if you believe you know somebody in your network who would be suited to this position please forward the details, we offer a competitive referral fee. We also have a presence on LinkedIn and Twitter, or you can sign to our mailing list on our website to be kept up to date with our roles.

Medella Life

As specialist recruiters in life sciences, our mission is to create a positive impact in the world. We place visionary people in thriving cultures where they can create a brighter future. Our impact and what that means to society is why we go the extra mile. We even baked it into our name, Medella, which means to heal. Pairing brilliant scientists with brilliant companies we find wildly exciting, and it drives everything