Top 8 Clinical research assistant Jobs in Monroe Ny

Clinical Research Coordinator
The Geneva Foundation —West Point, NY
- $55,000 - $60,000 a year
- Full-time
- Background check
- Microsoft Excel
- Mid-level
Quick Apply
Senior Clinical Study Manager (Hybrid)
Stryker —Mahwah, NJ
- $132,100 - $220,100 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Agile
- Senior level
- Health savings account
- AD&D insurance
Manager, Clinical Imaging Operations
Regeneron —Tarrytown, NY
- $128,600 - $210,000 a year
- Management
- 5 years
- Bachelor of Science
- Health insurance
- Dental insurance
Associate Director, Clinical Scientist, Ophthalmology
Regeneron —Tarrytown, NY
- $176,100 - $287,300 a year
- Internal Medicine
- Analysis skills
- Doctor of Philosophy
- Health insurance
- Dental insurance
Associate Medical Director, Clinical Development, Ophthalmology
Regeneron —Tarrytown, NY
- $243,600 - $329,400 a year
- Medicine
- Management
- Travel
- Health insurance
- Dental insurance

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Clinical Research Coordinator
The Geneva Foundation —West Point, NY
Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data.
$55,000 - $60,000 a year
Quick Apply
Part -Time Clinical Research Coordinator
Optum —Mount Kisco, NY
Prepare and be available for monthly recruitment calls with sponsors regarding prescreening updates, patient enrollment projections, barriers to recruitment,…
$24 - $43 an hour

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Clinical Research Coordinator

The Geneva Foundation -
West Point, NY

Quick Apply

Job Details

Full-time
$55,000 - $60,000 a year

Qualifications

Project team coordination
Data integrity assurance
Managing technical support teams
Microsoft Excel
Conference planning
Institutional Animal Care and Use Committees (IACUCs) guidelines compliance
Safety protocol adherence
Project documentation
GxP
Data validation techniques
Safety regulations
Filing
Mid-level
Research project design
Meeting scheduling
Data integrity and documentation
ICH guidelines
Bachelor's degree
Data quality monitoring
Data reporting support
Managing clinical research teams
Research compliance clinical trial records management
Infection control regulations
Meeting facilitation
Implementing research protocols
Project execution
Patient recruitment
Regulatory submissions
Productivity software
Clinical quality assurance standards

Full Job Description

About the Position

This role will specifically support the Baylor University–Keller Army Community Hospital Division I Sports Physical Therapy Fellowship. A premier post-professional training program focused on developing expert sports physical therapists through advanced clinical practice, leadership development, teaching, and research. As part of the MIRROR portfolio, fellows engage in meaningful clinical research designed to advance evidence-based care for Service Members and athletes. The program is expanding its research capacity and seeks a Research Coordinator to support the development, execution, and dissemination of high-quality research initiatives. This position offers a unique opportunity to contribute to an innovative military-academic partnership dedicated to excellence in rehabilitation and sports medicine.

About the Project

The position will support the Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) Program. This program was established to support the execution of clinically relevant research to advance the care of service members with non-combat related musculoskeletal injury (MSI). Headquartered at the Uniformed Services University of the Health Sciences (USU), MIRROR provides coordination and support of inter-service and inter-disciplinary partnerships across military treatment facilities (MTFs), military training centers (MTCs), and civilian academic centers to execute cutting-edge research in order to mitigate the burden of MSI on military readiness.

This is an on-site position assigned to the Keller Army Community Hospital at West Point, NY. A thorough government background check will be required.

Salary Range

$55,000 - $60,000. Salaries are determined based on several factors including external market data, internal equity, and the candidate’s related knowledge, skills, and abilities for the position.

QUALIFICATIONS

Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and posses a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines

RESPONSIBILITIES

Promote safety and confidentiality of research participants at all times
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives
Document all correspondence and communication pertinent to the research
Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization
Comply with all the rules and regulations as applicable to assigned duty station
Create and adhere to a data quality and quality assurance plan
Assist with interim and annual reports. S/he will be the primary liaison at the data collection site and will be responsible for explaining the project to military personnel associated with the study
Demonstrate proficiency in performing basic study related procedures
Complete required and applicable research training needed to complete research
Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)

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Refine Your Search

clinical research assistant jobs in monroe ny

Clinical Research Coordinator

Senior Clinical Study Manager (Hybrid)

Manager, Clinical Imaging Operations

Associate Director, Clinical Scientist, Ophthalmology

Associate Medical Director, Clinical Development, Ophthalmology

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