Top 75 Clinical research Jobs in Brighton Ny

Clinical Research Data Spec I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- University
- Organizational skills
- Experience equivalent to degree accepted
11d
Clinical Research Coordinator
ALLIANCE CLINICAL LLC —Rochester, NY
- $28 - $30 an hour
- Temporary
- CPR Certification
- Microsoft Excel
- BLS Certification
Quick Apply
8d
Manager, Clinical Research
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Office
- Master's degree
- University
11d
Human Subject Research Spec II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Word processing
- Mid-level
- University
Clinical Research Spec II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Mid-level
- Clinic
- Bachelor's degree
Human Subject Research Spec I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Hybrid work
- Word processing
- Mid-level
- University
Human Subject Research Coordinator I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Word processing
- University
- Bachelor's degree
Human Subject Research Specialist I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Remote
- Psychiatry
- Experience working with individuals with disabilities
- Adults
Financial Spec I, Clinical Trials
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Project Coordinator
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Weekends as needed
- Word processing
- Mid-level
- Driver's License
11d
Human Subject Research Coordinator II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Word processing
- Mid-level
- University
Clinical Trial Coordinator I/II FSP
Thermo Fisher Scientific —Rochester, NY
- $20 - $27 an hour
- Full-time
- Microsoft Word
- Computer literacy
- Mid-level
- Commuter assistance
- Paid parental leave
3d
Clinical Research Specialist II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Rotating shift
- Remote
- Psychiatry
- Experience working with individuals with disabilities
- Adults
Outcomes Specialist I, CHeT
University of Rochester —Rochester, NY
- $23.27 - $32.60 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- University
- Bachelor's degree
Clinical Research Regulatory Specialist II
University of Rochester —Rochester, NY
- $24.91 - $34.87 an hour
- Day shift
- Mid-level
- Office
- University
Sr Data Analyst
University of Rochester —Rochester, NY
- $64,200 - $96,200 a year
- Full-time
- 5 years
- HIPAA
- Mid-level
6h
Public Health Project Spec II
University of Rochester —Rochester, NY
- $23.27 - $32.60 an hour
- Full-time
- Microsoft Excel
- Mid-level
- Office
7d
Clinical Treatment Coordinator
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Medical office experience
- Mid-level
- 3 years
Clinical Research Assistant
ALLIANCE CLINICAL LLC —Rochester, NY
- $20 - $22 an hour
- Full-time
- Customer service
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Human Subjects Research Coordinator II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Management
- Word processing
- Mid-level

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Clinical Research Data Spec I

University of Rochester -
Rochester, NY

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Job Details

Full-time
$21.78 - $30.53 an hour
11 days ago

Qualifications

Data integrity assurance
Confidential information handling
Data validation techniques
Data integrity and documentation
Productivity software
Cross-functional collaboration
Cross-functional communication

Full Job Description

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.

Job Location (Full Address):

90 Crittenden Blvd, Rochester, New York, United States of America, 14642

Opening:

Worker Subtype:

Regular

Time Type:

Full time

Scheduled Weekly Hours:

Department:

400178 Cancer Center/Clin Trials Ofc

Work Shift:

UR - Day (United States of America)

Range:

UR URG 106 H

Compensation Range:

$21.78 - $30.53

The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.

Responsibilities:

Assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures. Coordinates with the Principal Investigators (PI), staff, and sponsor-designated contacts to resolve data inquiries as needed. Responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to Standard Operating Procedures (SOPs), and all applicable regulations and guidelines to ensure timely, accurate and compliant data reporting. Answers simple data clarifications (i.e. data queries) for each study.

ESSENTIAL FUNCTIONS

Inspects clinical data and research data from electronic records and other sources and assists study staff on entering this data into electronic medium for each assigned study. Supports the collection and analysis of research protocols and coordinates with the primary and sub-investigators. Reviews all data submitted for accuracy and completeness and determines if any actions are required to resolve any errors, omissions or discrepancies. Independently answers simple data clarifications and answers more complex data clarifications under guidance from management. Ensures all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines. Develops source data worksheets specific to each assigned study to ensure accurate source documentation.
Assists with the preparation and maintenance of electronic logs and data status updates to be presented routinely at PI Oversight meetings. Investigates and reports on data collection into an electronic data capture system in a timely manner according to protocol guidelines and department standard operating procedures (SOPs). Maintains screening, enrollment, and other sponsor and/or protocol specific logs, as required by protocol and department SOPs.
Works closely with the investigators and study personnel from all cross-functional teams to establish appropriate data collection methods to meet the needs for each assigned project. Designs and creates data collection forms and communicates regularly with the study team to optimize data review and handling processes. Ensures that appropriate quality assurance procedures are in place for error detection and correction.
Maintains currently knowledge and practice of all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines.
Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Demonstrates accountability for continuous learning and participates in protocol-related training as required.

MINIMUM EDUCATION & EXPERIENCE

Associate's degree and 1 year of relevant experience required
Bachelor's degree preferred

KNOWLEDGE, SKILLS AND ABILITIES

Skill in completing assignments accurately and with attention to detail required
Ability to process and handle confidential information with discretion required
Commitment to the University’s core values required
Ability to work independently and/or in a collaborative environment required
Understands and follows data integrity standards and processes required
Strong interpersonal, communication, and organizational skills required
Highly collaborative, works well in teams required
Proficient in MS Office (e.g. Word, Excel, and PowerPoint), email, internet required
Ability to understand and follow standard research protocols and procedures preferred
Knowledge of medical terminology preferred

The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.

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Refine Your Search

clinical research jobs in brighton ny

Clinical Research Data Spec I

Clinical Research Coordinator

Manager, Clinical Research

Human Subject Research Spec II

Clinical Research Spec II

Human Subject Research Spec I

Human Subject Research Coordinator I

Human Subject Research Specialist I

Financial Spec I, Clinical Trials

Project Coordinator

Human Subject Research Coordinator II

Clinical Trial Coordinator I/II FSP

Clinical Research Specialist II

Outcomes Specialist I, CHeT

Clinical Research Regulatory Specialist II

Sr Data Analyst

Public Health Project Spec II

Clinical Treatment Coordinator

Clinical Research Assistant

Human Subjects Research Coordinator II

I want to receive the latest job alert for clinical research in brighton ny

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