Clinical Research Assistant
Job Location:
Maplewood, WA - USA
Monthly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
At Headlands Research we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018 our rapidly growing company currently operates 20 sites across the US and Canada with plans for further expansion.
Location: Maplewood MN Site Name: Headlands Research - Twin Cities Full-Time Clinical Research
Are you an experienced clinical research professional with a passion for advancing medicine Join a leading integrated clinical research network dedicated to high-quality data patient-centered care and innovation in clinical trials.
Were seeking a Clinical Research Assistant for our clinical research site located in Maplewood MN.
Type: Regular Full-time Employee
Schedule: Mondays through Fridays 8:00am - 5:00pm
Pay Range: $18-27/hr *Dependent upon relevant experience certification and education.
Location: Onsite in Maplewood MN (no capabilities for remote or hybrid work)
Reports to: Site Director
Benefits: Our benefits package for full-time employees includes health insurance (medical dental and vision) Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA) Paid Time Off (PTO) a variety of disability accident and life insurance options as well as many more.
- Competitive pay annual performance incentives
- Medical dental and vision insurance
- 401(k) plan with company match
- Paid time off (PTO) and company holidays
- A mission-driven culture focused on advancing medicine and improving patient outcomes
Youll be part of a growing mission-driven organization that values its people. At our core were committed to bringing innovative medical treatments to patients fasterwhile creating an environment where employees thrive. If youre passionate about clinical research and ready to make a difference wed love to hear from you.
Responsibilities:
- Assist research coordinators in conducting clinical trial visits in compliance with study protocols
- Collect and record vital signs make study-related phone calls and document data in electronic systems
- Support subject screening enrollment and follow-up processes
- Review and verify study documentation for accuracy and completeness
- Maintain close communication with coordinators investigators and study participants
Requirements:
- Familiarity with medical terminology and basic laboratory procedures required
- Prior experience providing direct hands-on patient care preferred
- Clinical research experience preferred
- Comfortable using multiple electronic data entry systems
- Strong attention to detail time management and ability to work in a fast-paced regulated environment
- Excellent interpersonal skillsyoull be interacting with participants providers and sponsors
- Passion for improving patient outcomes through research
Headlands Research will never ask a candidate for personal identifiable information (date of birth social security number drivers license information etc) via email or messenger tools or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race color religion age sex national origin disability status genetic information protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process contact for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Required Experience:
Junior IC
