Job Description

Description This is a full-time, office-based position in Dallas, TX. Other key responsibilities: Create e-source documents, labels, and study-specific instructions. Host clinical planning meetings for each stage in study start-up. Develop study schedules. Order supplies, equipment, and dietary needs for studies. Liaise with CRU contracted services (e.g., clinical labs, ECG services). Train staff on study-specific procedures. Coordinate participant check-in, discharge, and issue resolution. Complete sample shipment documentation. Compile data tables and summaries. Ensure timely CRF completion and manage queries. Compile protocol and SOP deviations. Provide logistical feasibility for protocol development. Maintain accurate work records. Stay updated on FDA, GCP, and ICH requirements. Ensure client and participant confidentiality is maintained. Evaluate and revise SOPs. Assist with form reviews and activity plans on bedside date capture. All other duties as needed or assigned. Skills Data entry, Clinical, Research, Early Phase, Phase I, documentation review, IRB, Study Start Up, Close Out, Microsoft office Top Skills Details Data entry,Clinical,Research,Early Phase,Phase I,documentation review,IRB,Study Start Up,Close Out Additional Skills & Qualifications University/college degree (life science, pharmacy or related subject preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology). Fortrea may consider relevant and equivalent experience in lieu of educational requirements. 1-2 years of professional work experience with at least 1 year experience in clinical research. Basic Life Support Skills (BLS) or CPR/AED Certified. Experience Level Entry Level Pay and Benefits The pay range for this position is $25.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Dallas,TX. Application Deadline This position is anticipated to close on Mar 2, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options. Actalent

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