Job description

DESIRED QUALIFICATIONS:

• Clinical research experience and experience working in a medical center or private practice
• Experience using CTMS system and EDC program
• Excellent communication and problem-solving skills
• Ability to work effectively with a lead study coordinator on multiple assignments, in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail
• Bilingual - Spanish preferred

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Assist lead coordinator with all clinical research activities with moderate supervision
• Adhere to IRB approved protocols
• Participate in the informed consent process of study subjects
• Support the safety of clinical research patients/research participants
• Coordinate protocol related research procedures, study visits, and follow-up care
• Screen, recruit and enroll patients/research participants
• Maintain study source document
• Report adverse events
• Understand good clinical practice (GCP) and regulatory compliance
• Comply with institutional policies, standard operating procedures (SOPs) and guidelines

EDUCATION & EXPERIENCE (REQUIRED):

• Associate or an allied health degree in life science or related area or one year of relevant experience, or combination of education and relevant experience

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Demonstrated ability to multi-task.
• Demonstrated excellent organizational skills.
• Ability to communicate effectively both orally and in writing.
• Demonstrated experience working as part of a team.
• Relevant subject matter knowledge.

Job Type: Full-time

Pay: $27.88 - $31.25 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• On call

Application Question(s):

• What is a good email for our HR department to reach you at?

Education:

• Associate (Required)

Experience:

• Clinical Research: 2 years (Required)

Work Location: One location

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