We are a fast-growing, global, clinical research organization based in Dallas, TX. This position is for a candidate that is interested in making a career in the research sector.
We are seeking a dedicated and skilled Clinical Research Associate to join our dynamic team. The successful candidate will be responsible for managing and overseeing biospecimens procurement, ensuring compliance with regulations, and contributing to our innovative projects. They will also be assigned to manage clinical trial projects, work with lab services, feasibililty, logistics, kitting and other teams as needed.
The candidate should have excellent critical thinking and problem-solving skills, as well as time management. The applicant should also be extremely motivated and comfortable working independently or in a team setting. Must also be an outstanding multi-tasker with the ability to concurrently manage multiple client and site relationships across our global network for biospecimens and research sites. The right candidate should also be comfortable regularly speaking with senior doctors, researchers, and other personnel. Occasional travel may also be required for onsite monitoring and site audits.
We believe that the right person will become an integral part of our team and help us with our mission of providing better treatments and outcomes for patients across the globe.
Responsibilities:
Manage biospecimens procurement process including collection, processing, and documentation.
Plan, coordinate, and conduct clinical trials for medical devices in accordance with industry standards and regulatory guidelines.
Monitor clinical sites, ensuring adherence to protocols, SOPs, and ethical standards.
Collaborate with cross-functional teams including R&D, regulatory affairs, and quality assurance.
Prepare and submit necessary documentation, reports, and updates to relevant authorities.
Maintain accurate and complete records, ensuring data integrity and confidentiality.
Experience:
- Master’s Degree in Life Science field or related field is preferred, although may consider similar Bachelor’s Degree
- Prior CRO experience preferred - 2+ years
- Experience working with European pharmaceutical companies is a plus
- Customer service experience may also be helpful
We are a small and quickly growing company with a 20 year track record. For this position overtime may be required as needed. Candidate may be working on many aspects of a project including regulatory, project management with responsibility for client deliverables
Job Type: Full-time
Pay: $70,000.00 - $80,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
Experience level:
Schedule:
- 8 hour shift
- Monday to Friday
- Overtime
Education:
Work Location: In person