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Weekend Research Jobs in Ohio (NOW HIRING)

Position Overview Gabrail Cancer & Research Center, a PhaseWell Research site based in Canton, OH, is seeking a detail-oriented and patient-focused Clinical Research Coordinator (CRC) to support the ...

Job Type Full-time Description Position Overview Gabrail Cancer & Research Center, a PhaseWell Research site based in Canton, OH, is seeking a detail-oriented and patient-focused Clinical Research ...

Research Assistant

Columbus, OH · On-site

$18.50 - $25.50/hr

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I-IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely.

Unique opportunity to break into the Clinical Research space! * Work with a company that truly ... Consistent schedule, no overnights or weekends, Early Fridays, flex holidays, and more! **We can ...

No Weekend or Holiday Commitment Incentives & Benefits: TriHealth offers a comprehensive benefits ... The Manager of Clinical Research is responsible for establishing and maintaining a Research Program ...

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Weekend Research information

What is a Weekend Research job?

A Weekend Research job typically involves conducting research tasks during weekends, which can include data collection, literature reviews, experiments, or analysis depending on the field. These roles are often part-time and may be suited for students, professionals seeking extra income, or those unable to work during regular weekday hours. Weekend research positions can be found in academic institutions, private companies, or independent projects. Responsibilities and requirements vary by employer, but attention to detail, strong organizational skills, and the ability to work independently are usually important.

What are some common challenges faced by Weekend Research professionals, and how can they effectively manage their workload?

Weekend Research professionals often face the challenge of balancing tight deadlines and limited access to colleagues or resources during non-standard hours. To manage these challenges, it’s important to plan tasks ahead, utilize digital collaboration tools, and communicate clearly with team members about progress and needs before the weekend. Additionally, setting clear objectives and prioritizing tasks can help ensure efficient use of time, allowing for thorough and high-quality research even when support is limited.

What are the key skills and qualifications needed to thrive as a Weekend Researcher, and why are they important?

To thrive as a Weekend Researcher, you typically need strong analytical skills, attention to detail, and a relevant academic background or experience in research methods. Familiarity with data analysis tools, online research databases, and citation management systems is often required. Excellent time management, self-motivation, and clear written communication make someone stand out in this position. These skills and qualities are essential for producing accurate, timely, and well-organized research findings, especially within tight weekend deadlines.
What are the most commonly searched types of Research jobs in Ohio? The most popular types of Research jobs in Ohio are:
What cities in Ohio are hiring for Weekend Research jobs? Cities in Ohio with the most Weekend Research job openings:
Infographic showing various Weekend Research job openings in Ohio as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 64% Full Time, 30% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Research Coordinator

PhaseWell Research

Canton, OH • On-site

Full-time

Posted 4 days ago


Job description

Description:

Position Overview

Gabrail Cancer & Research Center, a PhaseWell Research site based in Canton, OH, is seeking a detail-oriented and patient-focused Clinical Research Coordinator (CRC) to support the execution of oncology clinical trials. With over 30 years of experience conducting Phase I–III clinical trials, Gabrail Cancer & Research Center has built a strong reputation for high-quality trial execution in oncology and hematology studies.

The CRC is responsible for the day-to-day coordination of assigned clinical studies, ensuring participant safety, high-quality source documentation, and clinical functions. This role is ideal for a clinical research professional who thrives in a fast-paced, highly regulated environment and is passionate about advancing innovative therapies

Requirements:

Key Responsibilities

- Study Coordination & Execution

o Coordinate and conduct primarily patient-facing and related study activities from site initiation through study close-out in accordance with protocol, GCP/ICH guidelines, FDA regulations, IRB requirements, and company SOPs

o Screen and enroll study participants

o Conduct and support subject visits, including follow-up and retention activities

o Maintain study supplies, equipment, and inventory

o Maintain thorough knowledge of assigned protocols, investigational products, and study requirements

- Clinical & Data Responsibilities

o Perform clinical procedures as trained and delegated, including vital signs, ECGs, phlebotomy, and basic laboratory processing

o Accurately document study activities in source documents and electronic systems following ALCOA+ principles

o Resolve queries in a timely manner

- Regulatory & Quality Compliance

o Maintain complete, accurate, and inspection-ready source documentation

o Support quality management and the data department to prepare for and participate in monitoring visits, audits, and regulatory inspections

o Complete required trainings, certifications, and study documentation timely

o Escalate protocol deviations, noncompliance, or quality concerns promptly

- Collaboration & Communication

o Maintain professional, timely communication with investigators, sponsors, CROs, monitors, and Gabrail Cancer & Research Center/PhaseWell team members

o Support site initiation visits, and study-related training sessions

Qualifications

- Education & Experience

o At least one of the following is required:

§ Medical Assistant, LPN/LVN, EMT, or similar clinical credential

- Skills & Competencies

o Working knowledge of GCP, FDA regulations, and clinical research operations

o Strong organizational skills with high attention to detail

o Excellent written, verbal, and interpersonal communication skills

o Ability to manage multiple tasks and adapt to changing priorities

o Proficiency with CTMS, EHRs, and Microsoft Office/Teams

o Ability to handle sensitive information with professionalism, and in compliance with HIPAA