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Clinical coordinator • charleston sc

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Clinical Research Coordinator

Alcanza Clinical ResearchCharleston, South Carolina, US
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Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico.We have established a strong pr...[internal_linking.show_more]

Clinical Psychologist

Professional Performance Development Group, IncNorth Charleston, South Carolina, United States
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A doctor of philosophy (PhD) or a doctor of psychology (PsyD) degree in clinical, counseling, or combined professional scientific psychology from a program accredited by the American Psychological ...[internal_linking.show_more]

Safety Coordinator

Frampton ConstructionCharleston, SC, US
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Safety Coordinator The Safety Coordinator supports the implementation and daily execution of Frampton Construction’s safety program across active jobsites.This role works closely with project teams...[internal_linking.show_more]

Options Coordinator

Toll BrothersCharleston, SC, United States
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Toll Brothers, America's Leading Luxury Home Builder, seeks an Options Coordinator for our office located in Greenwood Charleston, South Carolina.This position is on-site 5 days per week.The Option...[internal_linking.show_more]

Admissions Coordinator

Southeastern CollegeNorth Charleston, SC, USA
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The key role of Admissions Coordinators is to engage and on-board new students.The Admissions Coordinator is typically the first contact a prospective student has with Southeastern College.The natu...[internal_linking.show_more]

UNIV - Program Coordinator I - Surgery: Clinical Trials

MUSCCharleston, South Carolina, United States
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The Clinical Research Coordinator is responsible for conducting all aspects of clinical drug and device trials; patient data; and disease registries for the Department of Surgery as directed by the...[internal_linking.show_more]

Scheduling Coordinator

Generator Supercenter of CharlestonMt Pleasant, SC, US
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Scheduling Coordinator – Construction & Energy Projects.Full-Time | Monday–Friday | Fast-Paced Work Environment.North America’s #1 Generac dealer, providing high-quality backup power solutions and ...[internal_linking.show_more]

RPR Coordinator

Auto Dealership VII, LLCAutoNation USA Charleston
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Manage, write, and track all Reconditioning, PDI, and Inventory Recall’s.Responsible for communication, work allocation, supervision and training of a team of (or individual) Technicians and Porter...[internal_linking.show_more]

Installation Coordinator

Easy IceNorth Charleston, SC, United States
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Build Your Best Future With The Easy Ice Team.We're a growing company that provides an all-inclusive commercial ice machine subscription to business owners nationwide.We've been changing our indust...[internal_linking.show_more]

Marketing Coordinator

MungoNorth Charleston, SC, United States
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Mungo Homes has a new opening for a Marketing Coordinator on our Coastal Region team! This position is based out of the Charleston, SC office and is primarily responsible for supporting marketing e...[internal_linking.show_more]

Proposal Coordinator

TalenTrustNorth Charleston, SC, United States
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Established in 1900, Mead & Hunt is a nationally recognized professional services consulting firm, has a full-time position available for a Proposal Coordinator to work with our transportation infr...[internal_linking.show_more]

Licensing Coordinator

Harmony Senior ServicesCharleston, SC, United States
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The Licensing Coordinator is responsible for managing the end-to-end lifecycle of licenses, permits, and registrations for communities managed by Harmony Senior Services.This role ensures that all ...[internal_linking.show_more]

Parts Coordinator

Gerber Collision & GlassCharleston, SC
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The Parts Coordinator’s primary responsibility and accountability is to provide an exceptional and successful customer experience while proactively managing the process of ordering, receiving, stor...[internal_linking.show_more]

Production Coordinator

AerotekNorth Charleston, SC, United States
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Production Materials Coordinator.We are seeking a Production Materials Coordinator to support manufacturing operations through effective material planning, inventory control, and ERP execution.This...[internal_linking.show_more]

Utility Coordinator

Johnson, Mirmiran & Thompson, Inc.Mt. Pleasant, SC, US
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Johnson, Mirmiran & Thompson is a dynamic, 100% employee-owned consulting firm with more than 2,800 professionals, providing a full range of multidisciplinary engineering, architecture, information...[internal_linking.show_more]

Sales Coordinator

Holiday Inn Charleston - RiverviewCharleston, SC, US
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Health, Vision, Dental and PTO.NorthPointe Hospitality also offers a Daily Pay Option.Employees will be able to make secure, instant transfers of earned wages for a fee, before payday, whenever and...[internal_linking.show_more]

Guest Coordinator

Ulta Beauty, Inc.Mt Pleasant, South Carolina, United States
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At Ulta Beauty, some of the industry’s most highly-esteemed beauty leaders share themselves, as well as their expertise.Think robust organizational support.Ever-increasing levels of investment.And ...[internal_linking.show_more]

Office Coordinator

A1 Glass Of North Charleston LlcNorth Charleston, SC, US
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We are seeking a motivated and outgoing Office Coordinator to join our team.In this role, you will provide a variety of clerical and administrative support to our employees, ensuring the office run...[internal_linking.show_more]

Clinical Research Coordinator

Clinical Research Coordinator

Alcanza Clinical ResearchCharleston, South Carolina, US
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Description

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Key Responsibilities

Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Screening of patients for study enrollment;
  • Patient consents;
  • Patient follow-up visits;
  • Documenting in source clinic charts;
  • Entering data in EDC and answers queries;
  • Obtaining vital signs and ECGs;
  • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
  • Requesting and tracking medical record requests;
  • Updating and maintaining logs, chart filings;
  • Maintaining & ordering study specific supplies;]
  • Scheduling subjects for study visits and conducts appointment reminders;
  • Building/updating source as needed;
  • Conducting monitoring visits and resolves issues as needed in a timely manner;
  • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
  • Filing SAE/Deviation reports to Sponsor and IRB as needed;
  • Documenting and reporting adverse events;
  • Reporting non-compliance to appropriate staff in timely manner;
  • Maintaining positive and effective communication with clients and team members;
  • Always practicing ALCOAC principles with all documentation;
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned.
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.

Skills, Knowledge and Expertise

Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. Bi-lingual (English / Spanish) proficiency is a plus.

Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits

  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all.

We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these new therapies, and the entire medical community. Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life.

Alcanza is a culturally competent organization. We treat each other with dignity, creating an environment where all individuals feel welcome, heard, and respected for their unique perspectives and aspirations. We put considerable effort into finding exceptional employees who mirror the values most important to us: Inclusive, Impactful, Compassionate, and Determined.

Alcanza Clinical Research is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company.