Job Description
NEW CRA Opportunity-Medical Device experience required! This Jobot Job is hosted by: Audrey Block
Are you a fit? Easy Apply now by clicking the Apply button
and sending us your resume.
Salary: $100,000 - $140,000 per year
A bit about us: We are a well established consulting firm that provides solutions to medical device company, pharmaceuticals and biologics. We are hiring a CRA with medical device experience to join our team!
Why join us? Opportunity to wear different hats in a small company-lots of growth!
People management if interested
Strong benefits and compensation package
Opportunity to work in multiple therapeutic and diagnostic areas
Job Details Job Details:
We are looking for an experienced Clinical Research Associate (CRA) with a focus on Medical Devices to join our dynamic and innovative scientific team!
Responsibilities:
As a CRA, your primary responsibilities will include:
1. Planning and conducting clinical studies of medical devices to ensure they are safe and effective.
2. Monitoring clinical trials, ensuring they are carried out in accordance with the study protocol, standard operating procedures, good clinical practice (GCP), and the applicable regulatory requirements.
3. Coordinating with investigators and site staff to ensure the quality and integrity of the data collected in clinical trials.
4. Preparing and presenting study documentation including protocols, case report forms, and study reports.
5. Assisting in the development of study budgets and timelines.
6. Conducting site initiation, interim monitoring, and close-out visits.
7. Ensuring that adverse events and other clinical issues are reported promptly and accurately.
8. Participating in the preparation of regulatory submissions.
9. Liaising with internal and external stakeholders to ensure smooth execution of studies.
Qualifications:
The ideal candidate for the CRA role will have the following qualifications:
1. A Bachelor’s degree in a scientific or healthcare discipline.
2. A minimum of 2 years of experience in monitoring clinical studies, with medical device experience
3. Thorough knowledge and understanding of ICH guidelines, GCP, and relevant regulatory requirements.
4. Excellent communication and interpersonal skills, with the ability to interact effectively with team members, investigators, and site staff.
5. Strong organizational skills, with the ability to manage multiple tasks and meet deadlines.
6. Proficient in Microsoft Office Suite and clinical trial management systems.
7. Ability to travel as required for site visits.
If you are a motivated professional with a passion for improving patient care through scientific innovation, we invite you to apply. Join us and contribute to the development and delivery of next-generation medical devices.
Interested in hearing more? Easy Apply now by clicking the Apply button.
Job Tags
Part time, Interim role, Immediate start,