Clinical Data Coordinator

Job Description Clinical Research Data Coordinator I is primarily responsible for the completeness, timely delivery, and quality of clinical research data via data entry. Responsibilities + Manage and ensure accurate and timely retrieval and electronic data entry submission of protocol-driven data points to relevant research sponsors/organizations within the specified time frame. + Abstract and record essential physical and test data from internal and external sources. + Maintain a tracking system of study participants at relevant time points as deemed necessary. + Actively contribute toward tasks related to site monitor visits and/or audits conducted by the institution, industry sponsors, the FDA, and other authorities. + Correspond with personnel at external institutions to ensure that data from outside institutions are obtained on time and as specified by the protocol. + Actively contribute to the training and onboarding of Research Support Assistants. + Instruct trainees in proper data documentation and review the work of trainees for accuracy to ensure data entry is conducted properly and completely. Required Skills + 3+ years data entry and data management experience + 2+ years CTMS experience + Experience in clinical research highly preferred + Knowledge of EDC (Electronic Data Capture) systems Pay and Benefits The pay range for this position is $28.00 - $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 Orlando,FL. Application Deadline This position is anticipated to close on Apr 14, 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.