Join a team committed to impactful clinical research! We're seeking a Research Assistant I who thrives in a dynamic environment and is keen on contributing to the management and execution of diverse research projects. If you are well-organized, detail-oriented, and adaptable, this opportunity could be perfect for you.
Key Responsibilities:
Act as a versatile resource across various project teams, providing support wherever necessary to drive project success.
Engage with multiple functional areas based on business needs, including:
Research Operations
Community Health
Endpoint and Specialty Services
Site Operations
Data Management
Quality Control
Trial Master File
Prepare essential project documents like Master Plans, Resource Materials, and Meeting Minutes. Assist with document submission to the Trial Master File.
Manage communications with investigational sites, our team, and sponsors to address data queries and gather crucial documentation.
Track and support the administration of project-specific training as well as the entry and review of endpoint testing.
Contribute to the distribution and management of study materials and assist with query management and User Acceptance Testing (UAT).
Collaborate closely with team members to ensure deliverables are completed on time and issues are resolved promptly.
Serve as a study coordinator for designated projects as needed.
Maintain strict adherence to our Standard Operating Procedures, Good Clinical Practice guidelines, and relevant regulations.
What You Bring to the Team:
A minimum educational qualification of a GED or High School Diploma; a Nursing or Bachelor's degree is preferred.
At least one year of experience in a clinical research setting, or an equivalent combination of education and experience.
Familiarity with Good Clinical Practice and relevant FDA and ICH regulations.
Competence in Microsoft Office applications, especially in handling spreadsheets and documents.
Strong communication and organizational skills with an excellent eye for detail.
Ability to work collaboratively, manage multiple priorities, resolve conflicts, and solve problems effectively.
Benefits:
A comprehensive benefits package including medical, dental, and vision coverage.
Paid time off, including 11 paid holidays and a generous vacation policy.
A matching 401(k) plan, immediately vested, and competitive.
Access to on-site wellness facilities and a variety of monthly team-building and community events.
Options for flexible and remote work arrangements.
About Us:
We are a leading academic research organization specializing in clinical trial design and management, offering expertise across a variety of therapeutic areas. For over 30 years, we have designed and managed over 150 clinical trials with a focus on delivering meaningful results. Our community health division develops innovative programs that aim to empower communities and promote health and wellness.
Equal Opportunity Employment:
We celebrate diversity and are committed to creating an inclusive environment for all employees. We provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, genetics, and other protected statuses under applicable laws. We also accommodate disabilities as per ADA and other regulations. If you require special assistance, please contact our Human Resources team.
Apply Today!
Ready to make a significant impact in clinical research? If you meet the qualifications and are excited about the opportunity, we would love to hear from you. Please submit your application by the specified deadline. We look forward to your contribution to our team and our mission.
Employment Type: Full-Time
Salary: $ 19.00 23.00 Per Hour
