Clinical Research Coordinator - Patient Recruitment Specialist

This role is REMOTE but there are 3 sites in the Seattle area and site visits may be required--you MUST be located in the area.

Non-local applicants will NOT be considered.

• 6 month contract, 40 hours/week. There is opportunity for extension.

• $30+/hr

• Bachelor's degree preferred.

• Minimum 2 years of CRC experience.

Job Description

The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results.

Responsibilities

• Recruit and consent research participants.

• Conduct telephone or in-person interviews with participants, including screening for eligibility.

• Perform follow-up (by telephone, e-mail, and/or mail) with study participants.

• Prepare, mail, and process questionnaires and other study correspondence.

• Assist in tracking study participants using MS Excel.

• Keep accurate and detailed records and files of work.

• Review, edit, clean, and enter participant data into a database.

• Assist with literature reviews for proposal submissions and manuscript preparation.

• Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.

• Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.

Essential Skills

• Bachelor’s degree in science, social science, allied health science, public health, or medical field OR four (4) years of experience in a directly related field.

• High school diploma or General Education Development (GED).

• Experience in chart review, patient recruitment, EDC, EMR, clinical research, GCP, CRC, patient enrollment/consent, and data entry.

Additional Skills & Qualifications

• Bachelor’s degree in science, social science, allied health science, public health, or medical field (preferred).

• Minimum of 3 years in clinical research with a preference for relevant healthcare experience.

• Certification of CCRC or CCRP (preferred).

• Experience with EDC entry and query resolution (preferred).

Work Environment

This role is remote and the individual will be supporting three total sites. The position offers the opportunity to work in clinical research trials and support one of the leading healthcare providers in the US.

Pay and Benefits

The pay range for this position is $30.00 - $40.00

• 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 remote position.

Application Deadline

This position will be accepting applications until Nov 27, 2024.

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.