Clinical Data Coordinator

Job Title: Clinical Data Coordinator Job Description We are seeking a Clinical Data Coordinator to join the Clinical Trials Office at a renowned Cancer Center. This hybrid position involves working on-site for two days per week. The coordinator will provide direct clinical and data management support related to the conduct of clinical trials and the collection and reporting of study-related clinical data for clinical studies within an assigned disease team or area. Utilizing independent judgment and high-level decision-making, this role is responsible for data entry, monitoring visits, and patient scheduling for assigned disease team trials. Responsibilities Coordinate patient/study participant care from recruitment through off-treatment and follow-up phases, including scheduling and verification of appointments. Independently and accurately abstract, create, and maintain study participants' research records, ensuring all required data is collected, source verified, and entered into sponsor databases. Collaborate with study sponsor personnel and maintain effective communication. Utilize advanced computer skills with Excel and Word, and manage electronic medical databases. Maintain confidentiality and manage a variety of duties and shifting priorities in a changing environment. Ensure professional appearance and manner as well as an excellent attendance record. Essential Skills Two years of related work experience in clinical research or data management. Bachelor's degree in a related field. Intermediate to advanced proficiency in Excel, Word, and electronic medical databases. Impeccable interpersonal skills and ability to work both independently and as part of a team. Proven ability to multitask and be organized with meticulous attention to detail. Additional Skills & Qualifications Experience with Oracle software, Medidata Rave, EPIC, and ONCORE. Knowledge of federal regulations for HIPAA and IRB. Experience working in a clinical trials setting preferred. Oncology experience is a significant advantage. Completion of Good Clinical Practice (GCP) training. Work Environment This position offers a hybrid work environment with two days per week on-site. It provides an opportunity to support cutting-edge research while ensuring compliance with complex billing and regulatory standards. Remote candidates must reside in one of the following states: Alaska, California, Connecticut, Mississippi, Missouri, Nevada, New Mexico, North Dakota, South Dakota, or Wyoming. The workplace fosters professional growth and the chance to contribute to advancements in cancer research within a mission-driven environment. Job Type & Location This is a Contract to Hire position based out of New Haven, CT. Pay and Benefits The pay range for this position is $28.00 - $31.83/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 New Haven,CT. Application Deadline This position is anticipated to close on Aug 26, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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] for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.