Bilingual Clinical Research Coordinator

Clinical Research Coordinator

Working at a top-ranked research company, the Clinical Research Coordinator works under the general direction of the Principal Investigator to ensure protocols are conducted in accordance with the principles of Good Clinical Practice. The coordinator will coordinate clinical research studies and perform a variety of duties involved in the collection, compilation, and documentation of clinical research data. The coordinator will play a key role in coordinating all clinical trial activities, by following all applicable regulations governing the conduct of clinical trials. The primary skills include GCP proficiency, logical thinking, ability to prioritize, a can-do attitude, the ability to adapt quickly to changing business conditions, and strong interpersonal, and team-building skills.

The coordinator, working closely with study team members under the moderate direction of a Study Investigator, will have overall responsibilities for coordinating efforts with other study team members in order to achieve study objectives and corporate goals, including:

• Develop strong working relationships and maintain effective communication with study team members.
• Coordinate the day to day activities of the research visits by completing all assessments required for the visit (eg Vital signs, EKG, labwork).
• The Clinical Research Coordinator will ensure that subjects participating in a clinical trial are following the study protocol as directed.
• Maintain study source documents. Report adverse events.
• Ensure the subjects safety while on the study.
• Educate subjects on protocol, study intervention, study drugs, etc.
• Ensures the data collected is accurate, legible, organized by follow good clinical practices.

Requires a minimum of 2-3 yrs of experience in clinical research.

Strong interpersonal skills with attention to detail are a must. Demonstrated ability in positive relationship building, with strong verbal and written skills required.

Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.

Ability to travel for Clinic activities, attend investigator meetings, or vendor visits/audits, as required.

Familiar with the background of the study drug and requirements of the study

Have high ethical standards and professional honesty

Friendly and outgoing demeanor

Must demonstrate a passion for direct patient interaction

Demonstrate clinical competence, positive leadership, and ability to work collaboratively with a multi-disciplinary team

Prolonged periods of sitting at a desk and working on a computer

This is a Contract position based out of Albuquerque, NM.

The pay range for this position is $30.00 - $35.00/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)

This is a fully onsite position in Albuquerque,NM.

This position is anticipated to close on Jun 16, 2026.

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 process due to a disability, please email View email address on click.appcast.io for other accommodation options.

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.

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.

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.