fhi360 Clinical Research Associate (Spanish speaking) in Durham, North Carolina

The Clinical Research Associate (CRA) monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols. Reviews regulatory documents as required and prepares site visit reports. May be responsible for multiple projects and must work both independently and in a team environment. Participate in the study development and start-up process including reviewing protocols, designing and/or reviewing Case Report Forms (CRF), preparing Informed Consent Forms (ICF’s), developing study documents, organizing and presenting at investigator meetings, working with management on a monitoring strategy, and/or developing project-specific CRA training. S/he may participate in clinical training programs and maintain awareness of developments in the field of clinical research as needed. S/he may provide a benchmark of monitoring competence to inexperienced/less experienced colleagues. Prepares clinical documents, business correspondence, and procedural manuals. Maintain systems and process necessary to report trial status and activities; and to help ensure that quality, regulatory compliant clinical projects are conducted on time and within budget. Depending upon the level of experience, may become involved, when required, in other areas of study management and staff training and contributes to the review of sponsor/client’s and/or FHI 360’s systems and procedures as appropriate.

This job can be based anywhere in the US. Travel will be to sites in Puerto Rico, Costa Rica, Mexico, Brazil, Peru, Panama, Colombia, and Ecuador.


  • Assists in the preparation of routine protocols, informed consents, SOPs, and other appropriate documentation.

  • Monitors clinical trials to ensure subject safety and compliance with the study protocol, FDA regulations and ICH/GCP Guidelines, may be done with supervisor.

  • Coordinates necessary activities required to set-up, monitor, and close-out clinical trials sites.

  • Conduct site assessment, initiation, routine, and close-out monitoring visits, may require supervision.

  • Complete accurate monitoring visit reports.

  • Develops training materials and conducts training for study implementation.

Applied Knowledge & Skills:

  • Must be fluent in Spanish.

  • Exceptional attention to detail.

  • Effective clinical monitoring skills.

  • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology.

  • Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures.

  • Effective organizational and time management skills.

  • Effective interpersonal skills.

  • Proven flexibility and adaptability

  • Ability to work in a team or independently as required.

Problem Solving & Impact:

  • Must have a working knowledge of concepts, practices and procedures for conducting clinical research studies.

  • Solid knowledge of software programs used to collect data and track risk based monitoring parameters.

  • Ability to analyze and interpret data, identify errors and prepare reports.

  • Works on moderate to complex problems of diverse scope that require analysis or interpretation of identifiable factors.

  • Demonstrates good judgment in selecting methods and techniques for obtaining solutions.

  • Decisions may affect a work unit or area within a department.


  • Bachelor's Degree or its International Equivalent • Education, Health, Behavioral, Life or Social Sciences, International Development, Human Development or Related Field.


  • 3 - 5 years of previous clinical research experience.

  • Proficiency in Microsoft Office, spreadsheet software and other technology required.

  • Articulate, professional and able to communicate in a clear, positive fashion with clients and staff.

  • Must be able to read, write and speak fluent English.

  • Master’s degree or its international equivalent preferred.

  • Related prior work experience preferred.

Travel Requirements:

  • Greater than 50%

This job description summarizes the main duties of the job. It neither prescribes nor restricts the exact tasks that may be assigned to carry out these duties. This document should not be construed in any way to represent a contract of employment. Management reserves the right to review and revise this document at any time.FHI 360 fosters the strength and health of its workforce through a competitive benefits package, professional development and policies and programs that support healthy work/life balance. Join our global workforce to make a positive difference for others — and yourself.

Please click here to continue searching FHI 360's Career Portal.FHI 360 is an equal opportunity and affirmative action employer. FHI 360 is an equal employment and affirmative action employer whereby we do not engage in practices that discriminate against any person employed or seeking employment based on race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, marital status, disability, veteran status, genetic information or any other status or characteristic protected under applicable law.

FHI 360 is a nonprofit human development organization dedicated to improving lives in lasting ways by advancing integrated, locally driven solutions. Our staff includes experts in health, education, nutrition, environment, economic development, civil society, gender, youth, research, technology, communication and social marketing — creating a unique mix of capabilities to address today's interrelated development challenges. FHI 360 serves more than 60 countries and all U.S. states and territories.

As we evolve to meet the challenges of the future, we stand committed to the principles that have guided our organization for the last 40+ years. Our work continues to be grounded in research and science, strengthened by partnerships and focused on building the capacity of individuals, communities and countries to succeed.