Senior Clinical Research Coordinator
Iterative Health —Flowood, MS
- Full-time
- Vital signs
- 3 years
- Bachelor's degree
Quick Apply
Senior Project Safety Coordinator
The Haskell Company —Ridgeland, MS
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Construction site
- Health insurance
- Retirement plan
Quick Apply
1d
Senior Construction Quality Coordinator
The Haskell Company —Ridgeland, MS
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Construction site
- Health insurance
- Retirement plan
Quick Apply
3d

Discover related jobs

Based on your search for senior coordinator jobs.

Director of GME (Institutional Coordinator)
Confidential —Jackson, MS
Bachelor’s degree in Health Administration, Education, or related field (Master’s preferred). Assist faculty with curriculum implementation, resident…
$90,000 - $120,000 a year
Quick Apply
Program Director
One Voice MS —Jackson, MS
Track performance metrics, program outcomes, community efforts, field activity, deliverables, and other indicators needed to evaluate progress and impact.
$67,000 - $72,000 a year
Quick Apply
2d

Show more related jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Senior Scheduling & Fleet Planning Coordinator
Planes Companies —Columbus, OH
Confirm truck configuration, trailer readiness, and day cab vs. sleeper requirements before placement. Strong proficiency with scheduling systems, spreadsheets,…
$62,000 - $72,000 a year
Quick Apply
Sr Business Coordinator/ Accounts Payable Invoice Analyst-4
OhioHealth —Columbus, OH
Providing excellent customer service to internal associates/departments that have questions or need guidance on invoice processing; effectively answer supplier…

Show more jobs in cities nearby

I want to receive the latest job alert for senior coordinator in ridgeland ms

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

senior coordinator jobs near ridgeland ms

Senior Accountant jobs in Charlotte, Nc

Nyu Psychology Research jobs in New York, Ny

Senior Clinical Research Coordinator jobs in Austin, Tx

Senior Clinical Research Coordinator jobs in New York, Ny

Senior Clinical Research Coordinator jobs in Streeterville, Il

Research jobs in New Haven, Ct

Senior Clinical Research Coordinator jobs in Manhattan, Ny

Senior Living jobs in San Jose, Ca

Project Coordinator jobs in Salt Lake City, Ut

Senior Quality Coordinator jobs in Fridley, Mn

Clinical Research Coordinator jobs in St. Louis, Mo

Remote Quality Assurance jobs in Georgia

Senior Quality Coordinator jobs in Phoenix, Az

Senior Accountant jobs in Sacramento, Ca

Senior Project Coordinator jobs in San Jose, Ca

Senior Project Coordinator jobs in Los Angeles County, Ca

Community Engagement Coordinator jobs in Portland, Or

Senior Project Coordinator jobs in Denton, Tx

Senior Living jobs in Baltimore, Md

Senior Clinical Research Coordinator

Iterative Health -
Flowood, MS

Quick Apply

Job Details

Full-time

Qualifications

Data integrity assurance
Research project management
Vital signs
Informed consent
Research ethical considerations
Project documentation
Data validation techniques
EKG
Coaching
Filing
Clinical case management notes
Phlebotomy specimen handling
Project communication management
3 years
Patient safety
Data integrity and documentation
Schedule management
Bachelor's degree
Research safety & compliance
Medication supplies
Health information data integrity
Data quality monitoring
Healthcare privacy protection
Quality control
Project management in healthcare
Informed consent procedures implementation
Clinical assessment documentation
Health record chart audits
Medical record abstraction
Health information regulatory compliance

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 100+ clinical research sites across the US and Europe, accelerating the path to market for novel therapies. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

Senior Clinical Research Coordinator

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

We are seeking a full-time, experienced Senior Clinical Research Coordinator (Sr. CRC). The Sr. CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities:

Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management.
Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies
Schedule all patient research visits and procedures consistent with protocol requirements
Conduct patient visits as outlined within each study protocol
Dispense study medication, collect vital signs and perform ECGs
Perform blood draws, process and ship specimens per study protocol and IATA regulations
Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms.
Act as point of contact for study participants
Adhere to Research SOPs, Good Clinical Practices, and the study protocols
Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager and PI throughout course of the study
Ensure all safety data is reviewed by the PI in a timely manner
Maintain inventory of study equipment and supplies onsite at all times
Support other site staff with coaching on best practices for clinical trials processes, patient interactions, and project management
Work closely with Principal Investigators and referring positions to build understanding and enthusiasm for research opportunities for patients
Participate actively in communication of status and results to management; contribute and implement ideas to improve site performance
Assess problem situations to identify causes, gather and process relevant information, generate possible solutions; make recommendations to management to resolve the situations
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality
Schedule and prepare for monitor visits
Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy
New bullet ?

Iterative Health Expectations

All employees are expected to:

Perform quality work within deadlines with or without direct supervision
Interact professionally with other employees, customers and suppliers
Work effectively as a team contributor on all assignments
Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations

Qualifications

Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
Minimum 3 years of clinical research experience
Experience in phlebotomy preferred
Strong written and verbal communication skils
Ability to read, interpret, and apply clinic policies and research protocols
Ability to use standard office software
Must be able to lift up to 25 pounds

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

Quick Apply

Refine Your Search

senior coordinator jobs in ridgeland ms

Senior Clinical Research Coordinator

Senior Project Safety Coordinator

Senior Construction Quality Coordinator

Discover related jobs

Explore jobs in cities nearby

I want to receive the latest job alert for senior coordinator in ridgeland ms

Explore jobs in more locations

Senior Clinical Research Coordinator

Job Seeker Tools

Employer Tools

Browse

Stay Connected