Clinical Research Coordinator jobs in New York
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
Clinical Research Coordinator I
- Velocity Clinical Research, Inc.
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Vestal, NY
FULL_TIME
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Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Duties/Responsibilities- Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
- Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
- Implement research and administrative strategies to successfully manage assigned protocols.
- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
- Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
- Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
- Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs.
- Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
- Ensure staff are delegated and trained appropriately and documented
- Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
- Evaluate potential subjects for participation in clinical trials including phone and in person prescreens.
- Execute recruitment strategies defined by Clinical Research Team
- Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
- Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
- Promote respect for cultural diversity and conventions with all individuals.
- Bachelor’s degree with 1 year of relevant experience in the life science industry OR
- Associate’s degree with 2 years of relevant experience in the life science industry OR
- High School Graduate and/or technical degre with minimum of 3 years relevant experience in the life science industry
- Phlebotomy if applicable and required by state law
- Intramuscular dose administration and preparation if applicable and required by state law
- Demonstrated knowledge of medical terminology
- Demonstrated ability in the use of the following technology Computers, Microsoft Office software, fax, copier, and multi-line telephone.
- Demonstrated bility to work in a fast-paced environment
- Demonstrated verbal, written, and organizational skills
- Demonstrated interpersonal and communication skills
- Demonstrated ability to work as a team player
- Demonstrated ability to read, write, and speak English
- Demonstrated ability to multi-task
- Demonstrated ability to follow written guidelines
- Demonstrated ability to work independently, plan and prioritize with some guidance
- Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
- Must be detail oriented
- Demonstrated problem solving and strategic decision making ability.
- Proficient ability to accept individual responsibility for actions taken and demonstrate professionalism when judged, critiqued and/or praised.
- Sit or stand for long periods of time
- Travel locally and nationally
- Communicate in person and by a telephone
- Limited walking required
- Limited to lifting up to 30 pounds
- 5 Days Ago
Clinical Research Coordinator II
- Velocity Clinical Research, Inc.
-
Vestal, NY
FULL_TIME
- Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our...
- 8 Days Ago
Clinical Research Coordinator
- Brain Injury Research Center of Mount Sinai
-
New York, NY
FULL_TIME
- Start Date: Summer 2024Salary Range: $45,864 - $62,000The Brain Injury Research Center of Mount Sinai (BIRC-MS) conducts cutting-edge research focused on addressing the challenges of living with traum...
- 3 Days Ago
Clinical Research Nurse - Buffalo, NY
- Rochester Clinical Research
-
Buffalo, NY
FULL_TIME
- Job Summary: The Clinical Research Nurse works closely with the Principal Investigator managing study conduct from study selection through study closeout. The Clinical Research Nurse is responsible fo...
- 1 Month Ago
Clinical Research Coordinator jobs at Popular Companies
Clinical Research Coordinator
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Coordinator
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Coordinator
- Sanford Health
-
Fargo, ND
- Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
- 6/10/2024 12:00:00 AM
Clinical Research Coordinator
- Danbury Health Systems
-
Norwalk, CT
- Clinical Research Coordinator, Norwalk, CT Full-time, 40 hours; 8:30 am - 5:00 pm Nuvance Health has a network of conven...
- 6/10/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Peoria, IL
- Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
- 6/9/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Urbana, IL
- The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the dail...
- 6/8/2024 12:00:00 AM
Clinical Research Coordinator
- Sanford Health
-
Sioux Falls, SD
- Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
- 6/8/2024 12:00:00 AM
Clinical Research Coordinator
- Hackensack Meridian Health
-
Nutley, NJ
- Overview: Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients liv...
- 6/7/2024 12:00:00 AM
About New York
New York is a state in the Northeastern United States. New York was one of the original thirteen colonies that formed the United States.
New York covers 54,555 square miles (141,300 km2) and ranks as the 27th largest state by size.[3] The highest elevation in New York is Mount Marcy in the Adirondacks, at 5,344 feet (1,629 meters) above sea level; while the state's lowest point is at sea level, on the Atlantic Ocean.
In contrast with New York City's urban landscape, the vast majority of the state's geographic area is dominated by meadows, forests, rivers, farms, mountains, and lakes. Most of...
Source: Wikipedia (as of 04/17/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$64,330 to $86,739
Most Popular Cities in New York for Clinical Research Coordinator Jobs
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019