Bilingual Research Coordinator - Dalton, GA

Job Title: Clinical Research Coordinator - Relocate Dalton, GA for a Great Opportunity!!Job DescriptionThe Clinical Research Coordinator is responsible for utilizing Good Clinical Practices (GCP) in the screening, enrolling, and close monitoring of clinical research study subjects, ensuring protocol and regulatory compliance.Responsibilities+ Prioritize activities with regard to protocol timelines.+ Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.+ Maintain effective relationships with study participants and research personnel.+ Interact professionally with patients, sponsor representatives, investigators, and personnel.+ Coordinate and attend pre-study site visits, site initiation visits, and monitor visits.+ Identify adverse events (AEs) and Serious Adverse Events (SAEs) and notify Principal Investigator and Sponsor.+ Prescreen study candidates and obtain informed consent.+ Complete visit procedures in accordance with protocol.+ Train others and perform basic clinical procedures, such as blood draws and vital signs.+ Review laboratory results and other test results for completeness and alert values.+ Discuss study medication and procedures with Investigator and site staff.+ Record data legibly and enter in real-time on paper or e-source documents.+ Accurately record study medication inventory and patient compliance.+ Resolve data management queries and correct source data within sponsor timelines.+ Assist regulatory personnel with completion and filing of regulatory documents.+ Assist in the creation and review of source documents.+ Assist with planning and creation of recruitment materials.+ Assist in development of recruitment plan and contact potential candidates.+ Actively work with recruitment team in calling and recruiting subjects.+ Review and assess protocol for clarity and feasibility.+ Ensure all training and study requirements are met prior to trial conduct.+ Communicate clearly verbally and in writing.+ Attend Investigator meetings as required.+ Ensure adequate supplies have arrived on site for protocol initiation.Essential Skills+ Must be bilingual (English/Spanish).+ Must have 2+ years of CRC experience.+ Must have phlebotomy experience.Additional Skills & Qualifications+ Ability to understand and follow institutional SOPs.+ Excellent knowledge of medical and research terminology.+ Excellent knowledge of federal regulations and GCP.+ Ability to operate independently for most study activities.+ Ability to communicate effectively with a diverse team.+ Strong organizational, prioritization, and leadership skills.+ Strong computer skills with abilities using clinical trials database and MS Word and Excel.+ Critical thinker and problem solver.+ Friendly and outgoing personality.+ High level of self-motivation and energy.+ Excellent professional writing and communication skills.+ Ability to manage stakeholder communications and facilitate visits and meetings.+ Ability to work independently in a fast-paced environment with minimal supervision.Work EnvironmentThe position is based in an on-site clinic environment.Job Type & LocationThis is a Contract position based out of Birmingham, AL.Pay and BenefitsThe pay range for this position is $30.00 - $40.00/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 TypeThis is a fully onsite position in Birmingham,AL.Application DeadlineThis position is anticipated to close on Mar 26, 2026.About ActalentActalent 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.