Top 8125 Research study coordinator Jobs

Clinical Research Coordinator
Solaris Health Holdings LLC —North Charleston, SC
- Full-time
- Nursing
- BLS Certification
- HIPAA
Quick Apply
4d
Clinical Research Coordinator
Oura —Remote
- $65,450 - $90,000 a year
- Remote
- Mid-level
- Office
- 1 year
- Paid holidays
- Health insurance
2d
Research Coordinator I, Patient Operations
Sanguine Biosciences, Inc. —Remote
- $22 - $25 an hour
- Full-time
- Remote
- Spanish
- Google Workspace
- Computer literacy
Quick Apply
6d
Research Administrative Coordinator
Cardiovascular Associates of America —Remote
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick Apply
Clinical Research Coordinator
Blue Ridge Associates in Neurology —Remote
- Remote
- Nursing
- Patient monitoring
- HIPAA
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Research Assistant (Remote with travel)
Centricity Research —Remote
- Full-time
- Mid-level
- Travel
- In-person
- Continuing education credits
- Paid holidays
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Clinical Research Study Coordinator
DFW Healthcare MSO LLC —Dallas, TX
- Full-time
- Writing skills
- HIPAA
- Mid-level
Quick Apply
Research Recruitment Coordinator
Betting Hero —Remote
- Remote
- Google Workspace
- Administrative experience
- Continuous improvement
Quick Apply
13d
Community Brain Health Study Research Coordinator
GAP SOLUTIONS INC —Baltimore, MD
- $90,000 - $130,000 a year
- Full-time
- Clean driving record
- Patient monitoring
- HIPAA
Quick Apply
Clinical Research Coordinator
Intactus Enterprises & Management —Hollywood, FL
- $28.64 - $34.49 an hour
- Part-time
- Spanish
- Computer literacy
- HIPAA
Quick Apply
Research Study Coordinator 2-Obstetrics and Gynecology
University of Tennessee Health Science Center —Memphis, TN
- $4,182.12 - $5,000.00 a month
- Weekends as needed
- Anatomy knowledge
- Management
- Mid-level
Clinical Research- Sub Investigator ANP/PA
Aton Health —Kansas City, MO
- $100,000 - $125,000 a year
- Full-time
- Hybrid work
- Nursing
- Patient monitoring
- Certified Nurse Practitioner
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator Nurse RN
Curiex —Renton, WA
- $40 - $47 an hour
- Temporary
- Nursing
- Blood sampling
- RN License
- 401(k)
- Tuition reimbursement
Quick Apply
Certified Hand Therapist (CHT) – Occupational Therapist
Banner Physical Therapy —Surprise, AZ
- From $90,000 a year
- Full-time
- CPR Certification
- BLS Certification
- Mid-level
- Continuing education credits
- Loan repayment program
Quick Apply
Per Diem Inpatient Physical Therapist
Boston Medical Center —Boston, MA
- Part-time
- Background check
- CPR Certification
- High school
Quick Apply
Clinical Research Coordinator
Gilbert Center for Family Medicine —Gilbert, AZ
- $60,000 - $70,000 a year
- Full-time
- Background check
- Microsoft Outlook
- Customer service
- Health insurance
- Dental insurance
Quick Apply
Medical Assistant w/Degree
ROSS EDUCATION HOLDINGS INC —Jackson, MI
- Full-time
- Background check
- Classroom
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
5d
Board Certified Behavior Analyst Practicum (1000+ hours completed)
Mosaic Pediatric Therapy —Bon Air, VA
- $25 an hour
- Full-time
- Mid-level
- Master's degree
- Clinic
- Continuing education credits
- Health savings account
Quick Apply
Clinical Veterinarian (NIH/DVR)
Priority One Services, Inc —Bethesda, MD
- $148,000 - $166,000 a year
- Weekends as needed
- Microsoft Word
- Background check
- Microsoft Excel
- Relocation assistance
- Health insurance
Quick Apply
Board Certified Behavior Analyst Practicum (1000+ hours completed)
Mosaic Pediatric Therapy —Charlotte, NC
- $25 an hour
- Full-time
- Mid-level
- Master's degree
- Clinic
- Continuing education credits
- Health savings account
Quick Apply

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Clinical Research Coordinator

Solaris Health Holdings LLC -
North Charleston, SC

Quick Apply

Job Details

Full-time
4 days ago

Qualifications

BLS Certification
High school diploma or GED

Full Job Description

Description:

GENERAL SUMMARY

Clinical Research Coordinator works under Clinical Research Managers and are tasked with administering clinical trials. Responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.

Requirements:

ESSENTIAL JOB FUNCTION/COMPETENCIES

The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:

Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals.
Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol.
Coordination and management of the clinical trial, communication with sponsor and authorities, visit coordination, sampling, time management and product accountability.
Data collection and management, collection and development of source documents, use of CRFs, managing patient registration, AEs, filing and archiving, managing monitoring visits, dealing with queries.
Maintain accurate records of the receipt, inventory, and dispensation of study drug and obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol.
Patient visits, data collection and transcription/EDC, prepare for monitor visits, protocol adherence to include height, weight, blood pressure, respirations, pulse temperature, O2 saturation.
Schedule appointments and organize materials to be used during study visits and ensure that all required tests are completed for each study visit per protocol.
Includes initial study start-up information/ requirements, dissemination of updated Investigator’s Brochures, protocols and informed consent information, online training initiated by sponsor, review of correspondence throughout study.
Completes Source Documentation-which includes completing and uploading all necessary documents to CRIO and maintaining all charts properly.
Medical Assessment-includes obtaining information from patient or chart regarding name of medication, start and stop dates, dose, and indication.
Biological Sampling Collection/Packaging/Shipping – includes serum and/or tissue collection, processing, packaging and shipping per study specific requirements.
Case Report Form (CRF) Entries and Management – includes data entry, query resolution in paper and/or electronic CRFs.
Investigational Product (IP) Management – includes receiving IP supplies, IP accountability, monitoring of temperature controls, destructions or return of IP.
Develop and/or Maintain Essential Documents – includes study specific training documents, study specific logs, patient questionnaires, patient pill diaries, lab requisition forms, other study specific forms.
Supply Chain Maintenance-Supplies Inventoried, stocking, organizing, and resupply order placed as required. Completed in Envi system.
Study Coordination- rooming, administer questionnaires, scheduling scans, set up room for procedures and wipe and clean equipment after procedures and visits.
Obtain/Maintain all required training- GCP, IATA,CPR Occasionally help the study coordinators at other offices such as the surgery center.
Performs other position related duties as assigned.
Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.

CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS

BLS certification required, ACLS preferred.
License and certification as required by state.

KNOWLEDGE | SKILLS | ABILITIES

Knowledge of medical terminology, healthcare coding systems, and clinics functions.
Must be able to function in a team-oriented environment, display strong analytical, investigative, interpersonal and organizational skills, pay high attention to detail with consistent follow-through and be able to productively manage high volumes of work.
Knowledge of database management.
Maintain a working knowledge of all assigned study protocols and amendments.
Excellent verbal and written communication skills.
Skill in using computer programs and applications including Microsoft Office.
Delivers exceptional patient service throughout all interactions.
Excellent organizational skills and attention to detail.
Strong analytical and problem-solving skills.
Complies with all health and safety policies of the organization.
Complies with HIPAA regulations for patient confidentiality.
Ability to work independently and manage deadlines.
Ability to establish and maintain effective working relationships with patients, colleagues, physicians and the public; successfully manages interactions with challenging or difficult people.
Ability to deal compassionately, professionally, and courteously with patients, their families, physicians, and staff.
Ability to build relationships with patients and display empathy and compassion to patients.

EDUCATION REQUIREMENTS

High School Diploma or equivalent required.
Bachelor’s degree in a related field (biology, psychology, nursing or healthcare) preferred.

EXPERIENCE REQUIREMENTS

Experience with EPIC software preferred but not essential.
1-3 years of related experience preferred.

REQUIRED TRAVEL

Minimal travel required.

PHYSICAL DEMANDS

Carrying Weight Frequency

1-25 lbs. Frequent from 34% to 66%

26-50 lbs. Occasionally from 2% to 33%

Pushing/Pulling Frequency

1-25 lbs. Seldom, up to 2%

100 + lbs. Seldom, up to 2%

Lifting - Height, Weight Frequency

Floor to Chest, 1 -25 lbs. Occasional: from 2% to 33%

Floor to Chest, 26-50 lbs. Seldom: up to 2%

Floor to Waist, 1-25 lbs. Occasional: from 2% to 33%

Floor to Waist, 26-50 lbs. Seldom: up to 2%

Quick Apply

Refine Your Search

research study coordinator jobs

Clinical Research Coordinator

Clinical Research Coordinator

Research Coordinator I, Patient Operations

Research Administrative Coordinator

Clinical Research Coordinator

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Clinical Research Study Coordinator

Research Recruitment Coordinator

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Clinical Research Coordinator

Research Study Coordinator 2-Obstetrics and Gynecology

Clinical Research- Sub Investigator ANP/PA

Clinical Research Coordinator Nurse RN

Certified Hand Therapist (CHT) – Occupational Therapist

Per Diem Inpatient Physical Therapist

Clinical Research Coordinator

Medical Assistant w/Degree

Board Certified Behavior Analyst Practicum (1000+ hours completed)

Clinical Veterinarian (NIH/DVR)

Board Certified Behavior Analyst Practicum (1000+ hours completed)

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