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Clinical Research Coordinator
3 weeks ago
CB Wagner Services LLC Boca Raton, United StatesA growing research site management organization is searching for a part-time Clinical Research Coordinator to work 20-25 hours per week, facilitating and executing research activities of new and ongoing clinical trials. · Summary: · The Clinical Research Coordinator, under genera ...
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Clinical Research Coordinator
2 weeks ago
SQRL Boca Raton, United StatesHighlights · $55,000 - $75,000 salary based on CRC experience · Great benefits · Site that focuses on teamwork and high quality patient care · Promote into Sr. CRC, Site Manager, Site Director and more · The Company · Our client is a fast growing site network that currently has 1 ...
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Senior Clinical Research Coordinator
13 hours ago
Aquent Talent Deerfield, United StatesThe Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collabo ...
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Research Coordinator
2 weeks ago
Florida Atlantic University Boca Raton, United StatesFor more information on everything FAU has to offer, please visit · Position Summary: · Florida Atlantic University is seeking a Research Coordinator & Biorepository and Lab Administrator · The Research Coordinator & Biorepository and Lab Administrator reports to the Director of ...
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Clinical Research Coordinator
6 days ago
Aquent Talent Deerfield, United StatesOur client is seeking a Clinical Research Coordinator to work onsite at their Pearland, TX location. · Responsibilities: · Proficient with phlebotomy · * Decentralized/hybrid clinical trials experience · * Manages clinical research studies and adheres to Standard Operating Proce ...
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Clinical Research Coordinator
6 days ago
CB Wagner Services LLC Boca Raton, United StatesA growing research site management organization is searching for a part-time Clinical Research Coordinator to work 20-25 hours per week, facilitating and executing research activities of new and ongoing clinical trials. · Summary: · The Clinical Research Coordinator, under gene ...
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Clinical Research Coordinator
3 weeks ago
SQRL Boca Raton, United StatesJob Description · Job DescriptionOpportunity to join one of the fastest-growing Clinical Research site networks in the US The Boca Raton clinical research site has contributed significantly to advancing therapeutics in ultra-rare to common disease states. · Highlights · Play a ma ...
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Clinical Research Coordinator
2 weeks ago
Flourish Research Boca Raton, United StatesJob Description · Job DescriptionFlourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives We offer an excellent comprehensive benefits package, a supportive and collabo ...
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Senior Clinical Research Coordinator
2 weeks ago
ICONMA Deerfield, United StatesSenior Clinical Research Coordinator Location: Deerfield, IL/ Chicago, IL/HybridDuration: 12 months with possible contract to hire/ with possible extensionDescription: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operati ...
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Research Coordinator
3 weeks ago
Phoenix Clinical Research, LLC. Tamarac, United StatesJob Description · Job DescriptionClinical Research Coordinator · About us · Phoenix Clinical Research is a small business in HEALTH_CARE_MEDICAL in Tamarac, FL We are agile and innovative. · Clinical Research Coordinator · The Clinical Research Coordinator participates in all asp ...
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Clinical Research Coordinator 2
1 week ago
The University of Miami Boca Raton, United StatesCurrent Employees:If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review th ...
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Research Coordinator
1 day ago
ALLERGY & ASTHMA ASSOCIATES OF SOUTH FLORIDA, P.A. Fort Lauderdale, United StatesJob Description · Job DescriptionFlorida Center for Allergy and Asthma Research is looking for a hard working motivated individual to join our busy clinical Trial department in our Aventura office. Some level of medical assistant training would be a plus. · Requirements: High Sch ...
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Tenet Healthcare Corporation Boca Raton, United States Full timePosition Summary: · The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct of all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director. The CRC provi ...
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Clinical Research Coordinator
1 week ago
Clinical Research Center of Florida Pompano Beach, United StatesJob Description · Job Description · We are seeking an Entry-Level Clinical Research Coordinator to become an integral part of our team. We conduct clinical research in multi-specialty areas, including Urology, Gastroenterology, and Psychiatry. · We do Phase I-V clinical studies ...
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Clinical Research Coordinator
4 weeks ago
Clinical Research Center of Florida Pompano Beach, United StatesJob Description · Job DescriptionWe are seeking an Entry-Level Clinical Research Coordinator to become an integral part of our team. We conduct clinical research in multi-specialty areas, including Urology, Gastroenterology, and Psychiatry. · We do Phase I-V clinical studies for ...
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Clinical Research Coordinator
4 weeks ago
EVOLUTION RESEARCH GROUP Delray Beach, United StatesJob Details · Job Location · LOC001 BMR Brain Matters Research DelRay - Delray Beach, FL · CRC-FT · Title: Clinical Research Coordinator · Location: Delray Beach, FL · About us: · ERG is a leading U.S. based, privately held, independent clinical research site company, and provid ...
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Tenet Healthcare Corporation Boca Raton, United States Full timePosition Summary: · The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct of all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director. The CRC provi ...
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West Boca Medical Center Boca Raton, United States Full timePosition Summary: · The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct of all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director. The CRC prov ...
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Clinical Research Coordinator
5 days ago
Trinity Health Corporation Fort Lauderdale, United StatesEmployment Type: · Full time · Shift: · Day Shift · Description: · Job Summary: · conduct and oversee all aspects of clinical trials in the neuroscience Insititute. · This person will be responsible for the conduct of multiple clinical research activities. Ideal candidate will ha ...
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Clinical Research Coordinator
5 days ago
CAN Community Health Fort Lauderdale, United States: · Increase your chances of reaching the interview stage by reading the complete job description and applying promptly. · Job Title: Clinical Research Coordinator Date Prepared: 02/27/2017 · Status: Exempt EEO: Professional Date Revised: 01 /12/2023 · Statement of Purpose: T ...
Senior Clinical Research Coordinator - Deerfield, United States - ICONMA
Description
Senior Clinical Research Coordinator
Location:
Deerfield, IL/ Chicago, IL/Hybrid
Duration: 12 months with possible contract to hire/ with possible extension
Description:
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials.
CRC is responsible for the oversight, facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study.
The Sr.CRC works collaboratively with the entire team, sponsors, and Clinical Quality Associates to ensure productivity, quality, and timely completion of studies.
The Sr.CRC is expected to support, guide, train, demonstrate and lead clinical trial team members in the implementation of trial related activities.
The Sr.CRC applies critical thinking and creative problem-solving skills across a wide variety of clinical studies, and contributes to the development of new processes, procedures, tools and training to enhance clinical research activities and is accountable for adhering to quality standards.
Job Responsibilities:
Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants)
Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol
Creates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulations
Contributes to the training of clinical trial staff and accountable for compliance with the operational requirements of the clinical trial
Function as participants' primary point of contact, keeping them informed on the study progress, and facilitate involvement of other study team members, as needed (e.g., notify Principal Investigator of safety events)
Manage participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s)
Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal Investigator
Provides accurate and timely data collection, documentation, entry, and reporting in both Sponsor and Client databases
Supports the regulatory staff in the maintenance of regulatory documents in accordance with Client SOPs and applicable regulations
Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participants
Maintain regular contact with the Principal Investigator and team to review study details (e.g., progress, adverse events, enrollment)
Maintain study supplies and issue appropriate participant stipends
Ensures appropriate credentialing and training of the study team
Facilitate meetings with the study monitors, auditors, and investigators
Ensure timely response to queries and documentation of study-related issues
If applicable, disburses investigational product, manages inventory of equipment and study supplies, and provides patient education regarding administration, as necessary
Contribute to the development and implementation of tools, processes and training to enhance the administration and execution of clinical studies (e.g., GCP, ALCOA-C)
Accountable for site compliance with subject safety reporting, escalate issues
Demonstrate professionalism and apply basic leadership practices in all aspects of the role
Train and support study team members on a range of communication and teamwork best practices
Performs other duties related to the clinical trials as delegated by the Principal Investigator
Opportunity to be a part of clinical trials in a pharmacy.
Bringing the trials to the people at their local pharmacy.
Working on all trials within the delivery operation team.
Experience:
3-5 years in clinical trial space
Education:
BA Skills:
Working knowledge of ICH-GCP, US CFR, and HIPAA regulations
Experience working independently and making appropriate decisions to operationalize and move clinical trials forward
Experience overseeing multiple clinical trials concurrently, while maintaining attention to detail Experience prioritizing tasks and resources, meeting deadlines, and being adaptable to changing priorities
Preferred:
Proficient with phlebotomy
Decentralized/hybrid clinical trials experience
As an equal opportunity employer, ICONMA prides itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual orientation, citizenship, or disability.