Clinical Research Coordinator I Job at Mount Sinai Health System (New York)

Clinical Research Coordinator I

Supports Frenova Renal Research by providing administrative and clinical support...

Location

United States of America , Mishawaka

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

High School Diploma required
Associate’s Degree or Certified Medical Assistant preferred
2-4 years of experience of related experience preferred
Minimum 18 months experience in a medical setting and/or clinical research setting required
Willingness to obtain research specific training as needed
Ability to meet deadlines for multiple concurrent projects
Ability to understand and follow study specific protocol and direction
Ability to understand a patient medical record
Attention to detail required
Good computer skills including MS Excel

Job Responsibility

Utilizes experience and knowledge to act as a resource and provide on-going leadership and support to Clinical Research Assistant I
Conducts on the job training for Clinical Research Assistant I as requested
Researches and identifies research related issues and discrepancies
Obtains and prepares regulatory/essential documents throughout the duration of a study
Ensures documents and forms are compiled and submitted in a timely manner
Assists with maintaining constant communication with Institutional Review Boards, study sponsors, dialysis facility, practice and field staff
Assists with the contracting process, document preparation and execution
Interfaces with potential study subjects for the purpose of promoting participation in research studies
Assists with screening subjects for participation eligibility
Assists with and documents the obtaining of informed consent according to GCP

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

Fulltime

Clinical Research Coordinator I

The Clark Lab is seeking a full-time Clinical Research Coordinator to work on st...

Location

United States , New York

Salary:

58661.00 - 73530.00 USD / Year

Mount Sinai Health System

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Psychology, Neuroscience, or a related discipline
No experience required. One year of research experience preferred (prior experience in conducting psychiatric interviews and neuropsychological testing with patients or research participants is preferred)
A commitment of 2 years or more is preferred

Job Responsibility

Conduct participant recruitment, scheduling, and screening.
Conduct structured clinical interviews and neuropsychological test batteries.
Assist in the collection, organization, analysis, and review of experimental data for publication and presentation.
Assist with other lab-related duties

Fulltime

Clinical Research Coordinator I

CRC I is an entry-level position responsible for serving as the primary coordina...

Location

United States , Tucson

Salary:

Not provided

Tucson Medical Center

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a relevant field or equivalent experience
Good Clinical Practice, Human Research Protection Training, and Basic Life Support certifications required within 30 days of start date
Ability to understand clinical research theory, practices, and tools utilized
Above-average skill in the use of all Microsoft Office applications
Proficient with technology and comfortable learning new protocols, electronic data capture (EDC) systems, and electronic medical records (EMRs)
Knowledge of clinical care and assessment best practices
Knowledge of regulations and policies as they relate to patient research, evaluation, care, and information
Ability to maintain investigational product accountability
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations

Job Responsibility

Oversees, coordinates, develops, and manages the day-to-day clinical activities for specified research trials
Facilitate and coordinate daily clinical activities
Act as liaison between PI’s, ancillary departments, research subjects, sponsoring organizations and regulating bodies, vendors, brokers, and suppliers
Maintain regulatory documentation, including the Investigator Site File (ISF)
Prepare, submit, and track Institutional Review Board (IRB) submissions, amendments, and reports
Ensure investigational product (IP) accountability throughout the study
Coordinate study and Research Staff compliance metrics
Coordinate participant recruitment and outreach programs
Coordinate department quality and data integrity programs
Support research billing compliance and invoicing/financial administration

Fulltime

Clinical Research Coordinator I

The Clinical Research Coordinator I assists principal investigators or other stu...

Location

United States , Los Angeles

Salary:

61152.00 - 100464.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

1+ year experience in clinical trial coordination or computerized databases
High School Diploma or GED required
Bachelor's degree or Associate degree in related scientific field preferred
Certified clinical research associate/coordinator preferred

Job Responsibility

Assists principal investigators or other study team members with research studies
Assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Clinical Research Coordinator I-Neurosurgery

The Clinical Research Coordinator assists in the daily activities of clinical re...

Location

United States , New York

Salary:

58661.00 - 73530.00 USD / Year

Mount Sinai Health System

Expiration Date

Until further notice

Requirements

Bachelors or Masters degree in Science or closely related field
No experience required
One year of research experience preferred

Job Responsibility

Collects and records study data. Inputs all information into database
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements
Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires
Assists in preparing grant applications, IRB/GCO for submission and filings
Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews
Secures, delivers and ships clinical specimens as required by the protocol
Prepares for monitoring visits
Performs other related duties

Clinical Research Coordinator – Neurophysiology Research Core (CNRC)

The Clinical Research Coordinator will play a primary role in collecting data fo...

Location

United States , Brookline

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

A Bachelor's degree is required
2 years of experience is required
Previous experience with children with autism or other neurodevelopmental conditions is ideal
Previous experience working in a research setting (preferably paid professional experience, but may include undergraduate research experiences) is also a plus.

Job Responsibility

Consents and recruits patients for research studies through personal interviews and written communications with patients/families
Provides detailed background information regarding studies to families, communicates all policies and procedures, and responds to all inquiries
Evaluates suitability of prospective study candidates and makes selections based upon clinical knowledge of each study
Performs EEG and other data collection methods (e.g., ERP, eye-tracking) on participants aged 0-65 years
Serves as liaison to the families/patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them during data collection
Acts as a resource to study participants, addressing any concerns they may have
Troubleshoots resolution of any issues that may arise during data collection
Participates in the training of newly hired research study assistants, as required
Coordinates activities between the hospital and research laboratories to ensure correct testing/processing and send out instructions specific to the study
Communicates project policies and procedures to personnel

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

New

Clinical Research Coordinator

Clinical Research Coordinator (contingent workers) ICON plc is a world-leading ...

Location

Poland , Warsaw; Gdansk; Gliwice; Lodz; Zabrze

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a relevant field such as business administration, project management, or a related discipline
Experience in a similar role or environment, with a focus on project support
Experience in oncology therapeutic area strongly preferred
Strong analytical skills and attention to detail, with the ability to work effectively in a team
Excellent communication and interpersonal skills, with a collaborative approach to problem-solving
Proficiency in relevant software applications and tools to support project execution

Job Responsibility

Assisting in the development and implementation of project plans to meet organizational goals
Collaborating with team members to identify opportunities for improvement and innovation
Gathering and analyzing data to provide insights that support decision-making processes
Contributing to the creation of reports and documentation to track project progress
Building strong relationships with colleagues to enhance teamwork and communication across functions

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Parttime

New

Clinical Research Coordinator II

Job Description Must have RN licensure to qualify. PURPOSE AND SCOPE: Responsi...

Location

United States , Tupelo

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Graduate of a technical program in healthcare, specifically as a Registered Nurse
2 to 4 years of nursing experience, specifically as a Registered Nurse
Has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Research experience preferred
Critical care, nephrology and/ or cardiac nursing experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study's timeline of activities
Regularly evaluates the study subjects' condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

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Clinical Research Coordinator I

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