Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Related keywords
- Clinical Research Coordinator
- Clinical Research Trials Coordinator
- Research Clinical Coordinator
- Clinical Research Scientist I
- Remote Clinical Research Coordinator
- Clinical Research Specialist I
- Research Associate Clinical I
- Nurse Clinical Research I
- Clinical Research Coordinator I Registered Nurse
- Clinical Research Coordinator I With Transplantation
Some similar recruitments
Clinical Research Associate Jobs
Recruited by iCell Gene Therapeutics 8 months ago
Address Stony Brook, NY, United States
Clinical Research Coordinator Jobs
Recruited by SRG 8 months ago
Address Springfield, Illinois Metropolitan Area, United States
Clinical Research Coordinator Jobs
Recruited by Medasource 8 months ago
Address New York, United States
Research Scientist I Jobs
Recruited by Research Foundation for Mental Hygiene, Inc. 8 months ago
Address New York, NY, United States
Clinical Research Coordinator Jobs
Recruited by Hospital for Special Surgery 8 months ago
Address , New York, 10021
Research Coordinator Jobs
Recruited by Dotdash Meredith 9 months ago
Address New York, NY, United States
Director – Clinical Research, Skinceuticals Dmi
Recruited by L'Oréal 9 months ago
Address New York, NY, United States
Senior Clinical Research Coordinator
Recruited by Northwell Health 9 months ago
Address , Manhasset, 11030
$62,250 - $100,130 a year
Clinical Trials Nurse – Sarcoma Outpatient Setting, Nyc
Recruited by Memorial Sloan Kettering Cancer Center 9 months ago
Address , New York, 10017
$87,300 - $139,800 a year
Clinical Research Coordinator Jobs
Recruited by Columbia University Medical Center 9 months ago
Address , New York, 10032
$35 an hour
Clinical Research Coordinator Jobs
Recruited by Columbia University 9 months ago
Address , New York
$63,000 - $65,000 a year
Clinical Research Coordinator Ii
Recruited by Legacy Health 9 months ago
Address , Portland, 97210
Clinical Research Associate I (Part-Time)
Recruited by Binghamton University 9 months ago
Address Stony Brook, NY, United States
Clinical Research Associate-208919 Jobs
Recruited by Medix™ 9 months ago
Address Florida, United States
Clinical Research Coordinator Ii
Recruited by Roswell Park Comprehensive Cancer Center 9 months ago
Address Buffalo, NY, United States
Clinical Pathway Coordinator Jobs
Recruited by Roswell Park Comprehensive Cancer Center 9 months ago
Address Buffalo, NY, United States
Clinical Research Coordinator Jobs
Recruited by New York Medical College 9 months ago
Address Valhalla, NY, United States
Clinical Research Coordinator - 207479
Recruited by Medix™ 9 months ago
Address New York, NY, United States
Clinical Research Coordinator I
Company | Velocity Clinical Research, Inc. |
Address | Vestal, NY, United States |
Employment type | FULL_TIME |
Salary | |
Category | Biotechnology Research |
Expires | 2023-06-04 |
Posted at | 1 year ago |
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.
- The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
- Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
- Promote respect for cultural diversity and conventions with all individuals.
- Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
- 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.
- Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
- Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol.
- Execute recruitment strategies defined by Clinical Research Team
- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
- Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
- Implement research and administrative strategies to successfully manage assigned protocols.
- Ensure staff are delegated and trained appropriately and documented
- Evaluate potential subjects for participation in clinical trials including phone and in person prescreens.
- Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
- Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
- 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.
- Associate’s degree with 2 years of relevant experience in the life science industry OR
- Bachelor’s degree with 1 year 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 ability to work independently, plan and prioritize with some guidance
- Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
- Proficient ability to accept individual responsibility for actions taken and demonstrate professionalism when judged, critiqued and/or praised.
- Demonstrated ability to read, write, and speak English
- Demonstrated problem solving and strategic decision making ability.
- Demonstrated bility to work in a fast-paced environment
- Must be detail oriented
- Demonstrated verbal, written, and organizational skills
- Demonstrated ability to multi-task
- Demonstrated ability in the use of the following technology Computers, Microsoft Office software, fax, copier, and multi-line telephone.
- Demonstrated ability to follow written guidelines
- Demonstrated knowledge of medical terminology
- Demonstrated interpersonal and communication skills
- Demonstrated ability to work as a team player
- Travel locally and nationally
- Sit or stand for long periods of time
- Limited walking required
- Limited to lifting up to 30 pounds
- Communicate in person and by a telephone
-
Systems Analyst - Excel, Xml, Sql, Scripting
By CyberCoders At Salt Lake City, UT, United States 8 months ago
-
(Senior) Finance & Shared Services Manager
By Catholics For Choice At Washington, DC, United States 8 months ago
-
Paralegal - Probate Administration
By CyberCoders At Miami, FL, United States 8 months ago
-
Account Executive - Automotive Software
By ECW Search At United States 8 months ago
-
Construction Project Coordinator Jobs
By CyberCoders At River Falls, WI, United States 8 months ago