Certified Clinical Research Professional

Hey there, I'm Alexis. New here and figuring out how to make the most of JobzMall.

University of Michigan

Michigan State University

Promote good clinical practice in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection.
·      Prepare and/or review complex regulatory documents such as IRB applications, informed consents, complex amendments, progress reports, adverse event reports and protocol deviations per FDA and OHRP regulations.
·      Utilize effective communication skills and incorporate specific age, cultural, or developmental needs in patient and family interaction.
·      Prepare and participate in sponsor and external regulatory audits.
·      Participate in pre-study preparation, problem solving and maintenance of clinical trials.
·      Collect, process, and ship research specimens.
·      Maintain working knowledge of all applicable FDA guidelines and Good Clinical Practices.

Greear CV 2024.pdf

Clinical Research Coordinator

Alexis Greear

English

Budgeting

Risk Management

Financial Analysis

Quality Assurance

Strategic Planning

Project Management

Networking

Data Analysis

Planning

Communication

Time Management

Multitasking

Presentation skills

Organizational Skills

Negotiation

Budget management

Leadership

Risk assessment

Teamwork

Collaboration

Cultural competency

Program Evaluation

Regulatory compliance

Organization

Client Relations

Strategic Thinking

Problem-Solving

Team Coordination

Regulatory reporting

Decision-Making

Resource allocation

Stakeholder engagement

Technical Knowledge

Protocol Development

Subject Recruitment

Conflict Resolution

Emotional Intelligence

Time management

Critical thinking

collaboration

Adaptability

Empathy

Decision-making

Alexis Greear

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