Top 10 research associate Jobs in elyria, oh

Clinical Research Associate (Monitor)
The Clinical Trials Network —Cleveland, OH
- $67,000 - $73,000 a year
- 8 hour shift
- Hybrid work
- Background check
- Computer literacy
- Research
- Health insurance
- Dental insurance
Quick Apply
Experienced Clinical Research Associate - Full-Service
Syneos - Clinical and Corporate - Prod —Ohio
- $70,100 - $126,100 a year
- Full-time
- Mid-level
- Bachelor's degree
- Team management
- Employee stock purchase plan
- Health insurance
4d
Research Assistant - Brunswick, OH
Iterative Health —Brunswick, OH
- Full-time
- Inventory management
- High school diploma or GED
- Communication skills
Equity Research Associate
Northcoast Research —Cleveland, OH
- Writing skills
- Finance
- Analysis skills
Senior Equity Research Associate
Northcoast Research —Cleveland, OH
- Writing skills
- Mid-level
- Office
Equity Research Sales Associate (Hedge Fund Sales)
Cleveland Research Company —Cleveland, OH
- Full-time
- Writing skills
- Office
- Analysis skills
- Health insurance
- 401(k)
Quick Apply
Journeyman Research Laboratory Mechanic (RLM) Technician - Vacuum Facilities
Sierra Lobo, Inc. —Cleveland, OH
- Full-time
- Mechanic experience
- Mid-level
- Forklift

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Clinical Research Associate (Monitor)
The Clinical Trials Network —Cleveland, OH
Able to develop effective working relationships with site staff and colleagues. Ensure valid findings from the audit/inspection report are managed effectively…
$67,000 - $73,000 a year
Quick Apply
Eurofins TestOil Special Testing Laboratory Technician - Full Time Position
Eurofins TestOil —Strongsville, OH
College degree with science major or minimum of one year of experience working in a laboratory (Preferred). Run IC analysis on lab samples.
Quick Apply
9d

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Clinical Research Assistant
DraftHire —Columbus, OH
Our client is a long standing clinical research site in the Columbus, OH area that takes a truly unique patient-centric, service-oriented, approach to clinical…
$40,000 - $45,000 a year
Quick Apply
18h
Experienced Clinical Research Associate - Full-Service
Syneos - Clinical and Corporate - Prod —Ohio
Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of…
$70,100 - $126,100 a year
4d

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Clinical Research Associate (Monitor)

The Clinical Trials Network
Cleveland, OH

Quick Apply

Job Details

Full-time
$67,000 - $73,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Flexible schedule
Life insurance

Qualifications

Clinical research
Research
Bachelor's degree
Clinical trials
Regulatory audits
FDA regulations

Full Job Description

Clinical Trials Network (CTN) partners directly with physicians and medical practices to help them successfully launch and conduct clinical trials, often for the very first time. We provide end-to-end operational support, including feasibility assessments, regulatory start-up, infrastructure development, staff training, patient recruitment strategy, and ongoing study management.

Job Description

The Clinical Trial Monitor is responsible for managing the audit program, pre-audit planning, leading the audit, and following up internally and externally to get findings efficiently and effectively resolved. The range of audits in scope include but are not limited to sponsor audits and regulatory inspections directly impacting CTNx. The audit management specialist will also conduct internal audits and compose summary audit reports and effectively communicate the findings and observations to CTNx leadership. Each Compliance Monitor will maintain a set of sites and help train newly onboarded coordinators according to CTNx Coordinator Training Program.

Key Accountabilities:

Conduct SOP/GCP/Compliance Training with coordinators at site.
Ensure sites are adhering to CTNx’ s policies and procedures.
Perform on-site and remote audits as a quality assurance tool that is used to evaluate compliance and to ensure human subject protection and data integrity.
Complete internal audits based on audit schedule provided by Compliance Manager.
Work with sites to report protocol deviations for all studies.
Perform audits of CTNx systems and processes to ensure adherence to standards and requirements.
Define, refine, and manage our audit processes and procedures to ensure they continue to represent best practice in our industry. Maintain an in-depth knowledge of regulations impacting clinical research.
Prepare fully for upcoming audits and inspections to ensure all possible documentation, subject matter expertise, systems and other forms are evidence are fully available and in best order.
Conduct and host audits with a positive and professional demeanor and ensure best current audit practices are employed.
Ensure valid findings from the audit/inspection report are managed effectively by the organization, and in accordance with our procedures. Escalate significant findings to CTNx Management.
Coach and Support CRCs and PIs on a continuous basis based upon audit findings.
Work with study teams to formulate Corrective and Preventive Action Plans (CAPAs) based on audit findings, deviations, and events; conduct follow up audits to assess if the desired effect/change was achieved.
Use the quality assurance process as an opportunity for continuing education of study teams.
Track assigned research projects utilizing a risk-based assessment tool to prioritize research studies for in-depth review.

Knowledge, Skills & Attributes:

Previous knowledge and experience in audit and inspection management, and management of audit programs within the clinical trials space.
Minimum 1 year of relevant audit experience in a FDA Environment such as pharmaceutical, biotech or CRO company or similar environment required.
Comprehensive knowledge of the clinical trials process in addition to specific understanding of relevant regulations and guidelines including 21CFR-Part11 and ICH-GCP.
Strong critical thinking to analyze complex situations and discern critical issues and non-compliant situations and to recommend appropriate corrective and preventive actions.
Solid computer literacy, interpersonal skills, and ability to function independently within an environment that relies on technology for information and communication.
Knowledge of governmental regulations impacting clinical research.
Flexible, resourceful, and adaptable to rapidly changing environment with competing priorities.
Able to develop effective working relationships with site staff and colleagues.
Domestic Travel up to 40% (Ability to travel as needed to support audits and inspections)

Job Type: Full-time

Salary: $60,000.00 - $70,000.00 per year

Benefits:

401(k)
Dental insurance
Flexible schedule
Health insurance
Paid time off
Vision insurance

Schedule:

8-hour shift
Day shift
Monday to Friday

Education: Bachelor's (Required)

Experience: Clinical Trial Auditing: 2 year (Preferred)

Willingness to travel: 40% (Preferred)

Work Location: One location

Job Type: Full-time

Pay: $67,000.00 - $73,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Application Question(s):

Will you now or in the future require sponsorship to work in the U.S.?

Experience:

CRC or CRA: 2 years (Required)

Work Location: Hybrid remote in Cleveland, OH 44113

Quick Apply

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research associate jobs in elyria, oh

Clinical Research Associate (Monitor)

Experienced Clinical Research Associate - Full-Service

Research Assistant - Brunswick, OH

Equity Research Associate

Senior Equity Research Associate

Equity Research Sales Associate (Hedge Fund Sales)

Journeyman Research Laboratory Mechanic (RLM) Technician - Vacuum Facilities

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