Clinical Research Coordinator [C]

Phaxis

New York, NY

Apply

JOB DETAILS

SALARY

$43

SKILLS

Analysis Skills, Auditing, Case Report Form (CRF), Clinical Information, Clinical Information Systems, Clinical Laboratory, Clinical Research, Clinical Study Publications, Clinical Trial Management, Communication Skills, Computer Skills, Computer Software, Data Analysis, Data Collection, Data Entry, Data Formats, Data Quality, Database Administration, Documentation, Electronic Medical Records, Funding, Graphics Software, HIPAA (Health Insurance Portability and Accountability Act), IRB/IEC (Institutional Review Board/Independent Ethics Committee), Internet Search, Laboratory Testing, Maintain Compliance, Medical Office, Medical Records, Medical Research, Medical Terminology, Organizational Skills, Patient Registration, Publications, Quality Assurance, Regulations, Regulatory Compliance, Reporting Skills, Research Administration, Research Protocols, Risk Management, Spreadsheets, Statistics, Surgical Procedures, Trend Analysis, Word Processing, Writing Skills

LOCATION

New York, NY

POSTED

3 days ago

Duties:

Job Summary:
As an integral member of the MSK research team and in compliance with all regulatory, institutional, and departmental requirements, performs data collection, data entry and data analysis for research projects, databases, and research protocols within MSKCC. Ensures data quality and integrity during each phase of data collection and for each protocol assigned.

Data Collection/Data Entry:
-Utilizes appropriate methodologies to collect human subject information for a research project, database, and/or protocol.

Performance Expectations:
-Performs abstraction of data from source records in patient/human subject records (e.G., electronic medical record, laboratory or diagnostic test results, surgical/radiation treatments delivered);abstraction of data from publications, or data collection from outside physicians offices.
-If applicable, completes necessary data collection requirements for interdepartment research projects, databases, and/or protocols.
-Redacts source documentation as needed to ensure compliance with the Health Information Portability and Accountability Act (HIPAA) and other regulations.
-Uses research databases (e.G., sponsor electronic Case Report Forms, Medidata, RedCAP and Clinical Trials Management System (CTMS)) etc. Efficiently to complete assigned tasks.
-Enters data into the relevant data collection systems as per established protocol or project timelines.
-Ensures data are accurate and complete.
-Recommends changes/additions to established data fields, if needed.
-Performs queries in databases to identify missing data variables.
-Utilizes the Clinical Trial Management System (CTMS) with accuracy and timeliness registering patients and tracking visits.
-Stays up-to-date with system changes that affect job responsibilities.
-Attends required Clinical Research Administration (CRA) training, protocol training classes and systems training (e.G. CTMS Training).
-Attends departmental research meetings or service trainings, as needed.
-May recruit, consent, interview and collect relevant data from human subjects enrolled to non-therapeutic, minimal risk studies for selected departments at the discretion of the Manager.

Data Reporting:
-Generates reports to all necessary parties on the progress of the research project, database, or protocol.
-Facilitates and acts as primary liaison for monitoring visits and audits conducted by outside sponsors or internal CR QA.

Performance Expectations:
-Generates reports for Principal investigator, sponsoring agency, Institutional Review Board, DSM Committees, manager etc., as needed.
-Compiles data and assists in consolidating/analyzing data for presentation.
-Performs and/or responds to queries and/or assist with statistical analyses, as needed.
-Provides real-time updates on data entry status to study team and supervisor.
-Communicates to the manager or study team when there are any issues or questions regarding missing or incomplete participant data and identifies trends or gaps in source data availability or accuracy.
-Meets regularly with the manager or study team members to review study data progress.
-Reviews monitoring queries and enters appropriate data in the CRF.
-For complex queries, partners with clinical team (CTN, physician) to obtain responses to questions and then enters data in the database.

Quality Assurance:
-Participates in activities to ensure accurate and complete data and regulatory compliance.
*See attached Job Description for full details null

Skills:
Required Skills & Experience:
-Client will allow any amount of experience. If there is none, this should be escalated.
-Medical/Research Experience required with HS diploma/GED.
-Beginner written communication skills including composing written correspondence and presenting information in a clear and concise manner.
-Beginner analytical skills including the ability to abstract information from clinical documents and enter data into the appropriate database.
-Ability to enter data accurately.
-This position may require the incumbent to complete tasks of standard to moderate difficulty under limited supervision and/or to assist more senior research staff in working on more difficult assignments.
-Computer Skills: The ability to use a computer and software such as database management, spreadsheet, word processing and graphics applications.

Preferred Skills & Experience:
-Two-four (2-4) years of experience preferred.
-Medical/Research Experience preferred with Bachelor's degree.
-A strong familiarity with Internet searching.
-Medical terminology and an interest in science.
-Medical/Research Experience. Null

About the Company

Phaxis

We stand for PERSEVERANCE, as we refuse to quit when the journey gets tough. Your gold is our mission, and we search day and night to find it.

COMPANY SIZE

50 to 99 employees

INDUSTRY

Staffing/Employment Agencies

FOUNDED

2002

WEBSITE

https://phaxis.com/

Clinical Research Coordinator [C]

Phaxis

New York, NY

About the Company

Phaxis

Similar Job Searches