Job Title: Clinical Research Data Coordinator – Oncology Job Description The Clinical Research Data Coordinator plays a pivotal role in supporting oncology clinical trials by managing and maintaining accurate and timely data. This position ensures adherence to study protocols, regulatory requirements, and institutional policies, collaborating closely with clinical teams, sponsors, and regulatory bodies. Responsibilities + Extract and enter clinical data from medical records such as pathology reports, radiology results, and clinic notes into trial databases. + Maintain complete and accurate records for each study participant. + Track and report serious adverse events and protocol deviations. + Serve as the primary data coordinator for therapeutic and non-therapeutic oncology trials, including complex studies such as hematologic cancers and Phase I trials. + Attend study team meetings and provide updates on data entry timelines, database locks, and query resolutions. + Assist in the creation of source documents and completion of case report forms. + Prepare for internal and external audits and monitoring visits. + Support data deficiency corrections and develop corrective action plans. + Ensure compliance with federal, institutional, and sponsor regulations. + Collaborate with clinical, informatics, regulatory, and quality teams. + Participate in protocol-related training and contribute to process improvement initiatives. Required Skills & Experience + Clinical research experience + Clinical trial experience + Data management experience + Data queries proficiency + Oncology Clinical Research Data Management experience + Must have CRC experience + Must have data management/coordination experience in oncology trials Pay and Benefits The pay range for this position is $30.00 - $35.00/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 hybrid position in Houston,TX. Application Deadline This position is anticipated to close on Aug 8, 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.