JOB DETAILS

Clinical Research Coordinator - Medical Assistant (Unblinded)

CompanyCC DERMATOLOGY MSO LLC
LocationWarrenton
Work ModeOn Site
PostedApril 17, 2026
About The Company
Clear Choice Dermatology is a dermatology practice that is solely physician owned and operated. We aim to provide the highest level of skin care for residents in Oregon and Washington. Clear Choice Dermatology providers diagnose and treat every disorder and lesion encountered on the skin. We love caring for people of every age, race, and gender. We treat each person like they are family and take this approach when making treatment plans. By employing pharmacologic, surgical, and holistic techniques, we seek to free patients of pain, stress, and anxiety related to skin disorders. As board-certified dermatologists and dermatology trained physician assistants, we seek to provide the highest level of care for our patients in a kind and compassionate manner. We believe that the skin is the most vital system in the body and we focus on making patients feel great about their own skin. We would truly be honored to have you as our patient and look forward to meeting you in person.
About the Role

Description

We are seeking a dedicated and detail-oriented Clinical Research Coordinator with a Medical Assistant background to join our dynamic research team. This role offers an exciting opportunity to contribute to cutting-edge clinical trials, ensuring the integrity of drug accountability and proper dispensing of blinded medications to participants. The ideal candidate will be committed to maintaining high standards of accuracy, compliance, and participant safety in a fast-paced research environment.  


Key Responsibilities  

- Perform drug accountability activities, including inventory management, documentation, and reconciliation of study medications.  

- Dispense blinded study drugs to clinical trial participants in accordance with protocol guidelines.  

- Maintain accurate records of drug dispensation, returns, and wastage, ensuring compliance with regulatory standards.  

- Assist with participant visits, including preparation of study materials and collection of relevant data.  

- Support the research team in adhering to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.  

- Communicate effectively with participants, staff, and sponsors regarding medication procedures and study updates.  

- Ensure proper storage, handling, and documentation of investigational products.  


This position can be part time or full time. For part time about 10 hours every 2 weeks or Medical Assistant 30h per week. 

The position is about 20% Clinical Coordinator tasks and 80% Medical Assistant tasks- This is a new position with growing opportunity.  

Requirements

Qualifications

 

Skills and Qualifications  

- Certified Medical Assistant or equivalent healthcare certification.  

- Prior experience in clinical research, preferably with drug dispensing and accountability.  

- Knowledge of clinical trial protocols, GCP, and regulatory requirements.  

- GCP certified or able to become certified

- Familiar with SOP

- Strong organizational skills and attention to detail.  

- Excellent communication and interpersonal skills.  

- Ability to work independently and as part of a multidisciplinary team.  

- Proficiency in electronic data capture systems and Microsoft Office Suite.  

Join our innovative team committed to advancing medical research and improving patient outcomes. We offer a collaborative work environment, opportunities for professional growth, and comprehensive benefits to support your career development.

Key Skills
Clinical researchDrug accountabilityMedical assistantGood clinical practiceRegulatory complianceInventory managementData collectionElectronic data captureMicrosoft office suiteCommunicationOrganizational skillsAttention to detailProtocol adherence
Categories
HealthcareScience & ResearchAdministrative
Benefits
Professional growth opportunitiesCollaborative work environmentComprehensive benefits
Job Information
📋Core Responsibilities
The role involves managing drug accountability, dispensing blinded study medications, and maintaining accurate regulatory documentation. Additionally, the coordinator will assist with participant visits and ensure adherence to study protocols and Good Clinical Practice guidelines.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
81
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
30 hours
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