Monitoring Excellence Academy Program - Nuernberg, Deutschland - Labcorp

Labcorp

Geprüftes Unternehmen

Nuernberg, Deutschland

vor 3 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.

With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Fortrea is offering graduates and/or entry level applicants to join their team under a permanent contract and to be fully trained as a CRA as part of our
Monitoring Excellence Academy Program.

What is Monitoring Excellence Academy?

It is an internal training program aiming at developing you as a CRA to become fully operational to work for our Clinical Operations department.

Trainers, managers and clinical development team will support you to reach your professional goal to become a CRA while at the same time, you will be working and supporting our teams.

Responsibilities:

Monitoring site performance and creating action plans for sites not meeting expectations, in conjunction with the onsite CRA
Assist CRAs with the preparation for site visits (running reports, QC of files, resolving action items from previous visits)
Liaise with the project team and others to distribute and track clinical trial supplies to ensure sites have enough to continue recruitment
Perform Case Report Form review, query generation and resolution, assisting sites as needed
Document review and collection to ensure compliance and inspection readiness of TMF
Tracking and processing invoices from investigator sites against agreed contracts and budgets
Undertake project related administrative tasks (meeting minutes, recruitment tracking, site document preparation)
IHCRA may also be required to attend onsite monitoring visits as a comonitor with experienced CRAs to assist with tasks such as site regulatory file review and drug accountability

Education and Qualifications:

University degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Research experience in pharmaceutical or CRO industries may be considered
Good organizational and time management skills
Good communication skills
Fluency in German and English

Did you know?

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply.

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