Clinical Data Monitor (on-site)

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. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.

We are currently seeking a Clinical Data Monitor, to enter various data into databases and QC of labs as per the verification documents.

This is a full-time, office based position in Daytona Beach, Florida.

If you join us, you will work with some of the worlds leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.

Many data monitors are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, youll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know youll touch many patients lives around the world.

WHAT YOU WILL DO

You will utilize your skills, knowledge, and clinical judgement to enter clinical data into appropriate database via data entry screens by referring to source documents (image / PDF) along with entry of QC of lab ranges into databases.

Other key responsibilities:

• Assist with NTF (note to files) and quality issues.
• Assist with system QR (Quality Review) in a timely manner.
• Help with the organization and filing of lab reports and source documents.
• Ability and eye-for-detail to handle multiple tasks.
• Maintaining accurate records for all the tasks performed.
• Carry out all activities according to Standard Operating Procedures (SOPs) and Project Specific.
• Conventions within the framework of Quality Management and Good Clinical Practice (GCP)/ICH Guidelines.
• Undertake any other duties as required

YOU NEED TO BRING...

• High School diploma or equivalent is required.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• Excellent verbal and written communication skills, with good eye-for-detail and moderate 'typing/keyboarding' skills.
• Knowledge of Microsoft Office packages including Outlook, Word, PowerPoint, and Excel is essential.
• Must be highly organized, self-driven and highly motivated to work under pressure to meet demanding timelines.

The important thing for us is you are comfortable working in an environment that is:

• Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
• Changing priorities constantly asking you to prioritize and adapt on the spot.
• Teamwork and people skills are essential for the study to run smoothly.
• Technology based. We collect our data directly into an electronic environment.

What do you get?

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERG's (employee resource groups)

#LI-SE1

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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If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.