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Clinical research coordinator Jobs in Charleston, SC

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Clinical research coordinator • charleston sc

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Clinical Research Coordinator

Alcanza Clinical ResearchCharleston, South Carolina, US
Full-time
Quick Apply

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, VA, SC, TN, TX and Puerto Rico.We have established a strong... Show more

Home Health Clinical Services Coordinator (MCP Assistant)

Interim HealthCare - North Charleston, SCNorth Charleston, SC, US
Full-time +1

Home Health Clinical Services Coordinator (MCP Assistant) – LPN.Explore a fulfilling career path with a greater sense of purpose.As a Home Health Clinical Services Coordinator (MCP Assistant) at In... Show more

Market Research Participant

GL IncNorth Charleston, South Carolina
$15.00 hourly
Part-time +1

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of bet... Show more

 • Promoted

Clinical Psychologist - Charleston SC

MRG ExamsCharleston, SC, US
Full-time
Quick Apply

MRG Exams - Clinical Psychologist – Veteran Disability Assessments .We are seeking a dedicated Clinical Psychologist to join our team in performing medical assessments for U.Veterans as part o... Show more

UNIV - Research Program Coordinator I - Surgery: Transplant Surgery Research

Medical University of South CarolinaCharleston, SC, United States
$45,300.00 yearly
Full-time

UNIV - Research Program Coordinator I - Surgery: Transplant Surgery Research.The Department of Surgery, division of Clinical Trials, is actively recruiting for a Research Program Coordinator I.The ... Show more

UNIV - Clinical Research Coordinator - Department of Medicine: Division of Pulmonary

MUSCCharleston, South Carolina, United States
Full-time

The Senior Clinical Research Coordinator is responsible for the day-to-day coordination, management, and execution of complex clinical research studies in accordance with Good Clinical Practice (GC... Show more

Clinical Flow Cytometrist

Lighthouse Lab ServicesCharleston, SC, United States
$80,000.00 yearly
Permanent

Lighthouse Lab Services is the leading provider of laboratory personnel.Currently, we are working with a premier health system in Charleston, SC and we are seeking a Senior Flow Cytometry Scientist... Show more

Non Clinical - Non Clinical

InSync Consulting ServicesCharleston, SC, United States
Full-time

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Clinical Care Partner

Novant HealthMount Pleasant, SC, United States
Full-time

Coordinates and supports providers and nursing staff to ensure the delivery of safe, high-quality, and cost-effective patient care.Under the direction of a Registered Nurse, Advanced Practice Provi... Show more

Licensing Coordinator

Harmony Senior ServicesCharleston, SC, United States
Full-time +1

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 ... Show more

DMS Clinical Coordinator

Southeastern CollegeNorth Charleston, SC, USA
Full-time
Quick Apply

OVERVIEW: The Clinical Coordinator manages the clinical education component of the curriculum.Education, and Training: The Clinical Coordinator for Diagnostic Medical Sonography must have a minimum... Show more

Scheduling Coordinator

Generator SupercenterMount Pleasant, SC, United States
$45,000.00 yearly
Full-time

Scheduling Coordinator Construction & Energy Projects.Full-Time | MondayFriday | Fast-Paced Work Environment.North America's #1 Generac dealer, providing high-quality backup power solutions and re... Show more

Clinical Coordinator

SouthernMED PediatricsNorth Charleston, SC, United States
Full-time

What it means to be a Clinical Coordinator with Us.We value our families we serve, our communities and our team members.As such we need people like yourself who appreciate time spent with our famil... Show more

Medical Assistant Clinical Coordinator

Lowcountry Oncology AssociatesMount Pleasant, SC, United States
Full-time

Certified Medical Assistant Clinical Coordinator.Lowcountry Oncology Associates mission is delivering high-quality and compassionate cancer care in our community, for our community and by oncologis... Show more

Clinical Coordinator Dialysis Registered Nurse

TRC Total Renal Care IncCharleston AMG Specialty Acute
Full-time

Hospital Dr, Mt Pleasant, South Carolina, 29464-3251, United States of America.Clinical Coordinator Registered Nurse.ESRD) and chronic kidney disease.This role combines direct patient care with cli... Show more

RPR Coordinator

AutoNation Mobile ServiceCharleston, SC, United States
Full-time

Reconditioning, PDI, and Inventory Recall Manager.Manage, write, and track all Reconditioning, PDI, and Inventory Recall's.Responsible for communication, work allocation, supervision and training o... Show more

Finance Coordinator

Beemok HospitalityCharleston, SC, United States
Full-time

The Finance Coordinator supports the Assistant Director of Finance with the day-to-day administrative, transactional, and reporting work that keeps the property-level finance function running accur... Show more

Clinical Systems Manager

NovotechCharleston, SC, United States
Temporary

Clinical Systems & Technology Role.The Clinical Systems & Technology function provides operational leadership for the clinical business ownership of clinical technology, automation, and clinical re... Show more

Remote Clinical Review Pharmacist

Pharmacy CareersCharleston, SC, USA
Remote
Full-time

Remote Clinical Review Pharmacist – Work From Home | Evidence-Based Decisions | Flexible.Leverage your clinical knowledge in a fully remote Clinical Review Pharmacist role.Evaluate prescriptions an... Show more

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Clinical Research Coordinator

Clinical Research Coordinator

Alcanza Clinical ResearchCharleston, South Carolina, US
30+ days ago
Job type
  • Full-time
  • Quick Apply
Job description

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, VA, SC, TN, TX 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.