Crf Specialist I Early Phase Clinical Research - Dallas Tx

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 part-time, office-based position in Dallas, TX, working 20 hours per week. Scheduled shifts consist of 4-hour shifts on either first shift or mid-shift.** 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 and enter study data into case report forms using Metadata. * Collaborate with quality control and project management teams to ensure timely completion. * Address data questions and classifications during sponsor monitoring visits. * Resolve sponsor-generated data queries promptly. * Communicate effectively with data managers and CRAs, adhering to study protocols and SOPs. * 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. **Work Environment:** * Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment. * Occasional drives to site locations, occasional domestic travel. * Exposure to biological fluids. * Personal protective equipment required such as protective eyewear, garments, and gloves. **Physical Requirements:** * Ability to work in an upright and /or stationary position for 6-8 hours per day. * Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment. * Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. * Ability to access and use a variety of computer software developed both in-house and off-the-shelf. * Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. * Regular and consistent attendance. * Varied hours may be required. 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) * Experience coordinating people or processes; customer‑service experience helpful. Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).