Float - Clinical Research Assistant

Parkside Medical Group | The Onyx Group•Charleston, SC

4d•Hybrid

About The Position

The Clinical Research Assistant plays a key role in supporting Clinical Research Coordinators and Principal Investigators with Phase II–IV clinical trials, ensuring compliance with international research standards and regulations. This people-centered position is perfect for someone with a warm, approachable personality who enjoys working with diverse individuals. The role offers a great opportunity to learn and grow in a collaborative environment, with close supervision and guidance from experienced professionals.

Requirements

0-1 year experience.
Actively learning GCP, IATA standards, and SOPs; begins CMA certification training process if not previously completed.
Strong understanding of medical and clinical research terminology.
Excellent verbal, written & interpersonal skills.
Exceptional attention to detail and accuracy.
Checklist-based training on general clinical assessments and core research skills to ensure procedural consistency and team readiness.
Proficiency in Data Management and Informatics.
Adhere to Principles of Ethical Research Standards.
Highly organized individual with strong time management skills.
Continuous learning mindset and commitment to professional development.
Must be highly organized, utilize excellent verbal and written communication and be able to multi-task.
Requires excellent time management and communication skills and confidentiality.

Responsibilities

Recruit, screen and assist with enrolling study participants according to protocol requirements.
Obtain various biological samples, process and ship, as necessary and dependent on site specific needs.
Collect, record and maintain accurate study data in compliance with Good Clinical Practice.
Conduct medical record review.
Support participants throughout the study by answering inquiries, reinforcing study protocols, and escalating concerns to clinical staff when needed.
This role involves regular travel among the West Ashley & Goose Creek sites.
Collaborate with investigators, clinicians, quality assurance and sponsors.
Schedule and coordinate participant visits, assessments and follow-ups.
Input patient data into company systems.
Oversee organization and workflow of trials with meticulous attention to detail and ordering of priorities.
Navigate and address sponsor and study issues to resolution.
Maintenance of organized, complete study charts, and legible, accurate research documentation through written progress notes.
Have working knowledge of protocol including background, rationale, and description of investigational drug/device.
Thorough knowledge of Inclusion/Exclusion criteria with Investigator available for questions.
Submit all regulatory documents and correspondence to regulatory personnel in a timely manner.
Identify protocol problems and inform TCR Research Team of problems limiting recruitment and work on strategies to overcome these problems.
Participate in weekly site meetings.
Facilitates clear and consistent communication among clinical trial teams through phone, email, and face-to-face interactions to ensure alignment on procedures, updates and patient care.
Actively engages in cross training- including phlebotomy and interdepartmental collaboration to enhance versatility and comprehensive support during patient procedures.
Knowledge of the research process, the importance of adherence to protocols, and the accuracy needed in collection and documentation of research data.
Ability to read and understand the protocol, including any amendments, to ensure familiarity with study procedures and an understanding of the potential risks and side effects of the investigational product.
Ability to interact daily with physicians, nurses, study monitors and other sponsor representatives, administrators and other employees, community resources, patients and their families and significant others.