Clinical Research Coord II, Translational Neuroscience

Hugh Chatham Health; Winston-Salem (NC); On-site; USD 37,000 - 55,000; Full time

Benefits offered by this job

Health and welfare benefits

Flexible Spending Accounts

Adoption assistance

Retirement plans with employer match

Educational assistance

Job summary

Wake Forest Baptist Health is seeking a Clinical Studies Coordinator II - Translational Neuroscience to coordinate clinical research studies, support participant recruitment and study visits, and ensure regulatory compliance. The role collaborates with investigators to translate discoveries into patient care, requiring strong organization, communication, and data management skills.

Ideal candidates hold a Bachelor's degree with two years of clinical research experience (or equivalent) and may

Qualifications

• Bachelor's degree in a relevant field or equivalent combination of education/experience.
• Two years of clinical research experience or equivalent.
• Experience with regulatory compliance in clinical studies is preferred.

Responsibilities

• Coordinate clinical research studies and recruitment of participants.
• Support study visits and regulatory compliance.
• Collaborate with investigators to translate discoveries into patient care.
• Obtain informed consent and ensure sponsor data reporting requirements.
• Abstract data from medical records and complete CRFs.
• Mentor staff and contribute to quality improvement efforts.

Skills

Interpersonal skills

Oral communication

Written communication

Reading comprehension

Organizational skills

EPIC/WakeOne

OnCore/WISER

Clinical Trial Management System

Microsoft Office

Professional appearance

Intercultural sensitivity

Confidentiality

Education

Bachelor's degree in a relevant field

Two years of clinical research experience

Tools

EPIC/WakeOne

OnCore/WISER

Microsoft Office

Job description

Wake Forest Baptist Health is seeking a Clinical Studies Coordinator II - Translational Neuroscience to coordinate clinical research studies, support participant recruitment and study visits, and ensure regulatory compliance. The role collaborates with investigators to translate discoveries into patient care, requiring strong organization, communication, and data management skills.

Ideal candidates hold a Bachelor's degree with two years of clinical research experience (or equivalent) and may