Clinical Trials Research Coordinator I

Job Description

Job Description

Location: San Jose, CA - 95110Duration: 12+ months contractIntroduction

This role involves collecting data for clinical trials research with guidance. The position may also support clinical trials activities and research lab operations. The coordinator will assist in ensuring timely, accurate, and complete documentation of all research activities, including consent forms and reports. Additionally, the role involves supporting the development and implementation of routine quality control and assurance measures and providing feedback to research staff and management as instructed.

• Associate’s degree in Science, Public Health, Health Care Administration, or a directly related field OR a minimum of one (1) year of experience in clinical research or a directly related field.
• Proficiency in electronic health systems and databases used in research environments, or willingness to learn within 3 months of hire.
• Strong organizational and communication skills, both written and verbal.
• Proficiency in medical terminology.
• Attention to detail and accuracy.
• Ability to manage multiple tasks and demonstrate good prioritization and organizational skills.
• Flexibility and dependability.
• Ability to work effectively on cross-functional teams.
• Professional manner and appearance.
• Demonstrated skill in administrative tasks (e.g., filing, photocopying, faxing).
• Knowledge of GCP, federal, state, and local regulations, including HIPAA and company policies and procedures.
• Ability to work in a Labor Partnership environment.
• Prior work experience at the client or in the client's industry.

Applicants must be able to work directly for Artech on W2.

• Clinical trials experience preferred.

• Support the education of research staff and/or participants on standard protocols, documentation procedures, clinical best practices, or timeliness of submissions under guidance.
• Assist with the development and/or implementation of routine quality control and/or assurance measures.
• Document feedback to research staff and management as instructed.

• Opportunities for career advancement and maintenance as defined by the Clinical Trial Career Ladder Program.
• Supportive and collaborative work environment.
• Commitment to professional development and training.

For immediate consideration please click APPLY to begin the screening process with Alex.