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.

Are you looking for a stable position with a well-established company, a place where you could feel comfortable? Do you like working with people who are friendly and reliable? Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, building new possibilities for our clients.

In this role you will:

• Prepare study site specific materials in accordance with relevant SOPs

• Set up and maintain clinical investigator files and documentation.

• Data entry and maintenance of selected study tracking databases.

• Prepare study-related documents and other materials for delivery to archives, at appropriate intervals.

• Support payment activities including preparing invoices, reconciliation and creating purchase orders

• Perform other administrative duties as assigned

Education / Qualifications

• Life science degree

• Minimum 1 year of clinical trial related admin experience either as a Clinical Trial Associate, Clinical Research Coordinator, Study Coordinator or similar

• Basic understanding of GCP, ICH Guidelines and local regulations.

• A keen interest in Clinical Research

• Exceptional administration skills

• Experience in managing multiple priorities and able to meet deadlines

• Good social and time management skills

• Good interpersonal skills, oral and written

• Exhibit general computer literacy in excel

• Efficient and effective work in a matrix environment and ability to work independently

NOTE: this role will require the incumbent to work 4 days per week from the client office

Thomas Leader;[email protected];#LI-TL1;40

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea 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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