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 more than 90 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 CRF Specialist, to be responsible for transcribing and managing study data, ensuring accuracy, and collaborating with various stakeholders to meet project timelines and quality standards.
Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a full-time, office-based position in Dallas, TX.
If you join us, you will work with some of the world's 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 Specialists 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 practice your clinical skills and knowledge, you'll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
When the drug you worked with gets approved, you know you'll touch many patient's lives around the world.
WHAT YOU WILL DO
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of clinical research.
Other key responsibilities:
Transcribe study data from electronic or paper source into case report form.
Enter data using Metadata (the currently defined data management software).
Collaborate with the quality control team and project manager to ensure timely completion of case report forms.
Work with sponsors during monitoring visits to address data questions and classifications.
Provide timely follow-up and resolution to all sponsor generated data queries.
Conduct EDC screen reviews.
Communicate effectively with the data manager and CRAs.
Advocate for adherence to completion guidelines.
Support sites operations.
Understand and adhere to study protocols.
Strategize and apply SOPs effectively.
Constantly seek ways to improve the efficiency and quality of work processes.
All other duties as needed or assigned.
YOU NEED TO BRING... High school diploma or equivalent.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
1-2 years' experience in a research environment or related experience.
Strong attention to detail and accuracy.
Excellent communication and organizational skills.
Ability to work collaboratively with a team.
Experience in clinical research or related field is a plus.
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)
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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