Clinical Research Associate

Responsibilities

• Identify and select study sites for clinical trials.
• Perform regulatory and ethics committee submissions.
• Monitor clinical studies to ensure compliance with protocols.
• Manage site activities and local safety reporting as needed.

Essential Skills

• At least one year of clinical trials monitoring experience.
• University degree in life science.
• Excellent written and oral communication skills.
• Attention to detail.
• Good organizational and time management skills.
• Fully fluent in written and verbal English.
• Ability to work well within a team.
• Computer competency.

Additional Skills & Qualifications

• Experience in clinical research, clinical trials, pain management, and oncology.
• Experience in CRO, Pharma, and Clinical Monitoring.

Position Details

• Position type: Contract
• Location: Phoenix, AZ

Pay And Benefits

• Pay Range: $85.00 - $95.00/hr.
• Benefits: Medical, dental & vision, critical illness, accident, and hospital coverage, 401(k) retirement plan, life insurance, short and long-term disability, health spending account, transportation benefits, employee assistance program, time off/leave (PTO, vacation or sick leave).

Work Environment

• Remote work opportunities with occasional onsite visits.
• Significant travel required, up to 50%-60%.

About Actalent

• We are 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.
• We serve many of the Fortune 500.
• We are an equal opportunity employer.