Clinical Research Coordinator

About the role

The Clinical Research Coordinator is responsible for the planning, coordination, and execution of clinical research studies, including the collection and management of clinical trial data. This role supports the conduct of safety and efficacy studies under the supervision of the Principal Investigator and in accordance with approved study protocols, company standard operating procedures, and current Good Clinical Practice guidelines.

Responsibilities

• Plan, coordinate, and execute clinical research studies
• Collect and manage clinical trial data
• Support the conduct of safety and efficacy studies
• Work under the supervision of the Principal Investigator
• Ensure compliance with study protocols, company SOPs, and Good Clinical Practice guidelines
• Perform all assigned responsibilities necessary to support compliant, accurate, and efficient study execution

Requirements

• Education: Bachelor's degree in a relevant field (e.g., Biomedical Sciences, Pharmacy, Nursing)
• Experience: Minimum 2 years of experience in clinical research or related field
• Skills: Strong organizational and communication skills, proficiency in Microsoft Office, knowledge of Good Clinical Practice guidelines

Qualifications

• Ability to work independently and as part of a team
• Attention to detail and strong analytical skills
• Excellent interpersonal and communication skills

Benefits

• Competitive compensation package
• Flexible work schedule
• Professional development opportunities
• Health and wellness programs
• Employee referral program

Pay

Salary range: $50,000 - $75,000 annually, commensurate with experience

Schedule

Full-time position, Monday through Friday, 8:00 AM - 4:30 PM

Benefits

• Health insurance
• Retirement savings plan
• Employee assistance program
• Flexible spending accounts

Contact Information

To apply, please submit a resume and cover letter via our online application system. For more information about ALS, visit our website at [insert website URL].