Are you passionate about making a difference in the healthcare industry? Do you have a strong background in clinical research and a desire to contribute to groundbreaking medical advancements? Baptist Health South Florida is seeking a highly motivated and detail-oriented Clinical Research Admin to join our dynamic team. In this role, you will play a critical role in managing and coordinating our clinical trials and research studies, ensuring compliance with all regulatory and ethical standards. If you have excellent organizational skills, a keen eye for detail, and a commitment to promoting the highest quality of patient care, we encourage you to apply.
Manage and coordinate all aspects of clinical trials and research studies, ensuring they are conducted in accordance with regulatory and ethical standards.
Oversee the collection, organization, and maintenance of all research data and documentation.
Collaborate with physicians, nurses, and other healthcare professionals to facilitate the successful execution of clinical trials and studies.
Develop and maintain relationships with external stakeholders, including pharmaceutical companies and research institutions.
Ensure timely and accurate submission of all required regulatory documents and reports.
Monitor research budgets and expenses to ensure efficient use of resources.
Facilitate the recruitment and enrollment of eligible participants for clinical trials and studies.
Maintain comprehensive knowledge of current developments and trends in clinical research and healthcare industry standards.
Participate in the development and implementation of research protocols and procedures.
Provide guidance and support to research staff and ensure compliance with all relevant policies and procedures.
Communicate effectively with study sponsors, investigators, and research team members.
Contribute to the dissemination of research findings through presentations, publications, and other mediums.
Continuously evaluate and improve research processes to enhance efficiency and effectiveness.
Adhere to all confidentiality and privacy regulations in handling sensitive research data.
Act as a liaison between the research team and institutional review boards to ensure ethical considerations are met.
Maintain accurate and up-to-date records of all research activities and progress.
Participate in training and development opportunities to enhance knowledge and skills.
Comply with all safety and health regulations and policies.
Contribute to a positive and collaborative work environment within the research team.
Represent the organization and promote its mission and values in all interactions and activities.
Where is this job?
This job is located at Coral Gables, FL, USA
Job Qualifications
Bachelor’s Degree In A Related Field Such As Healthcare Administration, Nursing, Or Life Sciences.
Minimum Of 2-3 Years Of Experience In Clinical Research Administration, Preferably In A Healthcare Setting.
Knowledge Of Federal Regulations And Guidelines Related To Clinical Research, Including Hipaa And Good Clinical Practice (Gcp).
Strong Organizational And Project Management Skills, With The Ability To Prioritize And Manage Multiple Tasks Simultaneously.
Excellent Communication And Interpersonal Skills, With The Ability To Collaborate With Various Stakeholders Including Physicians, Researchers, And External Partners.
Required Skills
Time Management
Budget Management
Data Management
Quality Control
Report Writing
Project Coordination
Regulatory Compliance
Team Collaboration
Ethics
Protocol Development
Subject Recruitment
Investigator Support
Soft Skills
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Problem Solving
Time Management
Creativity
Organization
Teamwork
Adaptability
