Research Assistant (Clinical)

Headlands Research • Portland, OR

13d • Onsite

About The Position

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: Portland, OR | 🏥 Site Name: Summit Research | 🕒 Full-Time | 🧪 Clinical Research
We’re seeking a Clinical Research Assistant (RA) for our clinical research site located in downtown Portland. As an RA, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.
💼 The Role:
The Research Assistant is a vital member of the clinical research team, working under the supervision of the Site Director, Principal Investigator, and Clinical Research Coordinators (CRCs). This role supports the day-to-day operations of clinical trials by ensuring compliance with regulatory requirements and assisting in the smooth execution of study activities. The Research Assistant is integral in maintaining the integrity of data collection, patient care, and adherence to study protocols, contributing to advancements in clinical research.
Type: Regular Full-time Employee
Schedule: Mondays through Thursdays, 8:00am - 5:00pm
Location: Onsite in Portland, OR (no capabilities for remote or hybrid work)
Reports to: Clinical Research Manager

Requirements

• Bachelor’s degree preferred or equivalent experience
• 1–2 years in clinical research or healthcare environment.
• Familiarity with medical terminology, lab procedures, and research protocols preferred.
• Ability to collect, compile, and analyze data accurately.
• Strong interpersonal, verbal, and written communication skills.
• Proficiency in Microsoft Office and Electronic Data Capture (EDC) systems.
• Ability to prioritize tasks, meet deadlines, and work in a fast-paced environment.
• Comfortable working both independently and within a team.
• Understanding of HIPAA, FDA, GCP, and ICH guidelines (preferred).
• Basic computer literacy, with lab skills (e.g., blood draws, specimen processing) preferred.

Nice To Haves

• BLS/CPR, CNA, CMA, or similar certification.

Responsibilities

• Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.
• Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.
• Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Good Clinical Practice (GCP) guidelines.
• Assist in participant recruitment by prescreening electronic medical records, following up on referrals, and coordinating outreach efforts.
• Provide subject care, including explaining study procedures, answering questions, and monitoring diary compliance.
• Conduct study procedures, such as collecting vital signs, performing ECGs, and completing study questionnaires.
• Perform follow-up and reminder calls to ensure subject adherence to visits and study protocols.
• Assist with participant stipend tracking and processing.
• Perform blood draws (phlebotomy) and process biological samples, including shipping per study requirements.
• Maintain laboratory equipment, supplies, and temperature control systems, ensuring compliance with study protocols.
• Generate and file weekly temperature reports for laboratory systems
• Enter and verify study data in Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), and other databases.
• Address system-generated queries and perform quality control checks to ensure data accuracy and completeness.
• Assist with case report forms (CRFs) and source document completion, including query resolution under study coordinator guidance.
• Maintain and organize participant charts, Investigator Site Files, and other regulatory documents.
• Support clinical research coordinators (CRCs) by filing, scanning, and faxing required documents.
• Clean, stock, and maintain exam rooms and department supplies to ensure readiness for participant visits.
• Participate in investigator meetings, study teleconferences, and trainings.
• Assist with onsite or remote clinical research monitor visits.

Benefits

• 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
• Competitive pay + annual performance incentives
• 401(k) plan with company match
• Paid time off (PTO) and company holidays
• Opportunities for professional development and career growth
• A mission-driven culture focused on advancing medicine and improving patient outcomes

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 11-50 employees