Clinical Research Coordinator

Jobtailor; New York (NY); On-site; USD 42,000 - 64,000; Full time

Job summary

Jobtailor is seeking a detail-oriented data entry and clinical research support specialist in New York. The role focuses on collecting and entering data for research projects and ensuring data integrity across studies.

You will support patient-facing activities, coordinate study visits, and collaborate with MSK teams to ensure timely data capture and reporting. Strong communication and adaptability are essential.

Qualifications

• Experience in a healthcare, research, academic, or other setting that involves working with data, information, or structured processes is a plus
• Ability to make timely, thoughtful decisions
• Takes ownership of responsibilities and follows through on commitments
• Willingness to take action and embrace new opportunities and challenges
• Ability to adapt, recover from setbacks, and find solutions to obstacles
• Interest in medical terminology, science, and clinical research
• Excellent written and verbal communication skills
• Enthusiasm and dedication to MSK's vision, mission, and values
• Flexibility may be required depending on the needs of the team
• Commitment: At least 2 years

Responsibilities

• Collect, abstract, and enter data for research projects, databases, and clinical trial protocols
• Maintain the quality, accuracy, and integrity of research data throughout the life of a study
• Support patient-facing research activities, including assisting with patient consent, coordinating study visits, or working with patients in the clinical setting, as applicable
• Partner with research and care teams across MSK to ensure data is captured accurately and on time
• Generate reports and communicate updates on research project, database, and clinical protocol progress
• Create and improve databases, data collection forms, patient calendars, tracking tools, and other research resources
• Help ensure research activities comply with applicable Institutional, State, and Federal regulations
• Coordinate clinical research protocols and serve as a key point of contact for assigned studies, as applicable
• Report to Clinical Research Leadership

Skills

Data Abstraction

Database Management

Data Quality Assurance

Clinical Trial Protocols

Data Entry

Research Data Reporting

Tools

Data Tracking Tools

Patient Calendars

Data Collection Forms

Job description

• Collect, abstract, and enter data for research projects, databases, and clinical trial protocols
• Maintain the quality, accuracy, and integrity of research data throughout the life of a study
• Support patient-facing research activities, including assisting with patient consent, coordinating study visits, or working with patients in the clinical setting, as applicable
• Partner with research and care teams across MSK to ensure data is captured accurately and on time
• Generate reports and communicate updates on research project, database, and clinical protocol progress
• Create and improve databases, data collection forms, patient calendars, tracking tools, and other research resources
• Help ensure research activities comply with applicable Institutional, State, and Federal regulations
• Coordinate clinical research protocols and serve as a key point of contact for assigned studies, as applicable
• Report to Clinical Research Leadership

Requirements

• Experience in a healthcare, research, academic, or other setting that involves working with data, information, or structured processes is a plus
• Ability to make timely, thoughtful decisions
• Takes ownership of responsibilities and follows through on commitments
• Willingness to take action and embrace new opportunities and challenges
• Ability to adapt, recover from setbacks, and find solutions to obstacles
• Interest in medical terminology, science, and clinical research
• Excellent written and verbal communication skills
• Enthusiasm and dedication to MSK's vision, mission, and values
• Flexibility may be required depending on the needs of the team
• Commitment: At least 2 years

Core Competencies

Demonstrates expertise in data collection, management, and reporting within clinical research settings, ensuring compliance with regulations and maintaining data integrity. Strong communication skills and adaptability are essential for supporting patient-facing research activities and collaborating with multidisciplinary teams.

Highest-signal resume keywords

• Data Collection
• Clinical Research Protocols
• Regulatory Compliance
• Patient Interaction
• Report Generation

ATS Optimization Keywords

Hard Skills

• Data Abstraction
• Database Management
• Data Quality Assurance
• Clinical Trial Protocols
• Research Data Entry

Soft Skills

• Decision Making
• Ownership
• Adaptability
• Communication
• Enthusiasm

Industry Keywords

• Healthcare
• Research
• Clinical Research
• Medical Terminology
• Academic Research

Tools & Technologies

• Data Tracking Tools
• Patient Calendars
• Data Collection Forms