Job Summary
The Remote Clinical Research Associate will play a crucial role in managing clinical trials related to medical devices. This position involves overseeing the planning, execution, and closeout of clinical studies to ensure compliance with regulatory standards and protocols.
Responsibilities
- Coordinate and monitor clinical trials to ensure adherence to study protocols and regulatory requirements.
- Conduct site visits to assess study progress, gather data, and maintain relationships with investigators and study staff.
- Assist in the development of study materials, including protocols, informed consent forms, and case report forms.
- Ensure accurate documentation and reporting of study data and adverse events.
- Provide support during audits and inspections by regulatory agencies.
- Collaborate with cross-functional teams to ensure successful trial execution.
- Identify and solve issues that may affect study timelines and quality.
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, or a related field.
- Previous experience in clinical research, preferably within medical device trials.
- Knowledge of GCP regulations and clinical trial processes.
- Strong organizational and communication skills.
- Proficiency in data management and clinical trial software.
- Ability to work independently and within a team in a remote environment.
- Willingness to travel as needed for site visits.
Providence Medical Technology provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
