Job Title: Clinical Research Coordinator Job Description The Clinical Research Coordinator is responsible for coordinating multiple research protocols and serving as a liaison with local investigators and sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations to achieve a fundamental understanding of human subject research. Responsibilities + Practice and adhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement'. + Complete routine training assignments as required during employment. + Perform routine operational activities for multiple research protocols. + Liaise between site research personnel, industry sponsors, and supervisor. + Collaborate closely with various site departments and teams, including finance, hospital administrative representatives, and the local IRB, if applicable. + Coordinate schedule of assessments from initial submission of feasibility until study closeout. + Review study design and inclusion/exclusion criteria with physician and patient. + Ensure the protection of study patients by verifying informed consent procedures and adhering to protocol. + Ensure the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitor data for missing or implausible entries. + Develop study-specific tools for source documentation when not provided by sponsor. + Collect, complete, and enter data into study-specific case report forms or electronic data capture systems. + Generate and track drug shipments, device shipments, and supplies as needed. + Ensure timely and accurate data completion. + Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations. + Communicate all protocol-related issues to appropriate study personnel or manager. + Attend study-specific on-site meetings, investigator meetings, conference calls, and monthly CRC meetings, as required. + Review and respond to any monitoring and auditing findings. Essential Skills + Knowledge of organizational policies, standard operating procedures, and systems. + Emerging understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment. + Basic understanding of medical terminology. + Effective communication skills. + Strong organizational skills and time management. + Basic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping. + 2 years of experience in clinical research. + Hospital experience. + Experience conducting industry trials. + Ability to pull records from an EMR. + Bachelor’s Degree. Additional Skills & Qualifications + 1+ years of relevant experience preferred. + Clinical competencies in performing clinical tasks, including ECG, phlebotomy, and the process of handling, centrifuging, storing, and shipping of specimens. + Self-motivated with a meticulous eye for detail. + Interpersonal skills. Pay and Benefits The pay range for this position is $25.00 - $28.00/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 Humble,TX. Application Deadline This position is anticipated to close on Jul 11, 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.