Register
Recruit Create CV

Clinical Study Nurse Coordinator Jobs

Clinical Study Coordinator - Chatham, Ny
By Lightship At Chatham, NY, United States
Required knowledge, skills, and abilities
Supporting supply and inventory management, including:
Updating the inventory management system
Bachelor's Degree in Life Science or healthcare-related field, or requisite combination of education, training, and experience
Understanding and complying with all regulations, policies, and guidelines applicable to clinical research, including GCP, FDA, and IRB requirements
Collecting study data and completing data entry / case report forms in various electronic systems and on paper
Study Coordinator Ii Jobs
By DLH Corporation At Durham, NC, United States
Assist with data collection, electronic data entry and audit checks.
Ability to multi-task and manage time effectively
Ability to pivot to meet changing requirements as needed
Experience drafting regulatory submissions for IRB
Experience with protocol development and consent writing
Experience working at a clinical research site and/or conducting federal clinical research
Study Coordinator Jobs
By DLH Corporation At Bethesda, MD, United States
Experience with adverse event reporting per clinical standards and FDA requirements strongly preferred
Work with Data Managers and Data Team members for forms preparation, and completion of adjudication procedures
Experience working in an academic or NIH research environment preferred
Knowledge of medical terminology preferred
Bachelor's degree req'd with 2 years experience in public health, clinical research or related field.
Implement study activities in accordance with NIH and FDA regulations
Study Support Coordinator I
By Clinical ink At United States
Support the organization with daily tasks including user management, site management, equipment requests, data entry and report generation
Provide support for front-end client activities across multiple clinical research studies
Work closely with clients to ensure all data required for study start-up is collected and maintained
Provide details and information to clients in response to inquiries regarding study support and set-up
Update project-related internal databases and electronic files to ensure accuracy
Assist with special department projects
Medical Center- Nurse Coordinator, Ambulatory Services/ Clinical Nurse Ii
By University of Maryland Medical System At Baltimore, MD, United States
Provides symptom management strategies to a defined patient population in collaboration with physician.
Ensures development and implementation of effective discharge plans and concurrently and retrospectively reviews patients for medical appropriateness and risk management issues.
Highly effective presentation skills are required to deliver educational information regarding breast health.
Assists patients with authorizing and pre-certification of insurance coverage for tests as ordered as part of the treatment plan.
Develops patient education materials and overall process for practice setting-based patient education
Accountable for compliance with regulatory requirements and holds others accountable
Clinical Study Manager Jobs
By Lexitas Pharma Services At United States
Must have excellent management and communication skills (written and verbal), strong problem-solving skills, and be detail oriented
Manages vendors, including the implementation and coordination of vendor’s Scope of Work (SOW).
Manages study budget and timelines. Identifies, resolves, or escalates issues involving study timelines and deliverables
Relevant experience as a CRA preferred
Study planning and set-up, maintenance, and close-out experience.
Must have a solid understanding of clinical research operations including GCP and regulatory requirements and operational procedures
Part-Time Contract Clinical Study Coordinator
By NeuroPace At San Francisco Bay Area, United States
General understanding of clinical documentation management and document control
Manage the eTMF (Trial Master File) system
Minimum of 2 years relevant work experience
Medidata and eTMF experience preferred
Previous experience in a clinical or regulatory department highly preferred.
Proficient in MS Word, Excel and Adobe PDF. Experience with clinical trial software systems, including eTMF, preferable
Study Coordinator Jobs
By McKesson At Nashville, TN, United States
You will present in weekly protocol meeting to investigators, research staff, and management
You will maintain case report forms tracking management database
You will reports patient visit and data entry information in financial tracking system.
Knowledge of FDA guidelines and GCP is required.
Interpersonal skills, detailed-oriented and meticulous.
Computer skills with ability using clinical trial databases, electronic data capture, MS Access or Excel
Clinical Study Manager Ii
By Tech Observer At New Jersey, United States
Assist the team with filing and data entry as appropriate
Demonstrates ability to manage all points of the clinical study project
Supports and effectively multi-tasks different and complex assignments and responsibilities.
Strong oral and written communication skills.
Investigates and determines solutions to difficult, problematic situations; escalates issues as necessary.
A Bachelor's degree in Life Sciences is acceptable.
Clinical Study Coordinator (Remote)
By Guardant Health At Palo Alto, CA, United States
Facilitate the coordination and management of clinical studies
Knowledge of ICH/GCP guidelines, including basic understanding of regulatory requirements in other countries, preferred
A minimum of 1 year experience in a CLIA, CAP-accredited laboratory preferred
A minimum of 1 year of experience as a clinical research coordinator preferred, ideally in a lab or device setting
Working knowledge of local, state, and federal laboratory regulations
Effective interpersonal skills and ability to effectively communicate (verbal and written) across all levels of the company
Clinical Program Nurse Coordinator Iii
By Sutter Health At , San Francisco, Ca $80.50 - $106.26 an hour
Equivalent experience will be accepted in lieu of the required degree or diploma.
DEPARTMENT SPECIFIC CERTIFICATION & LICENSURE
Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans.
Nurse Coordinator Clinical/Ukhc
By University of Kentucky At , Lexington, 40508, Ky $26.00 - $45.70 an hour
Skills / Knowledge / Abilities
BSN preferred. Previous management or coordinator experience within Endoscopy is preferred.
Does this position have supervisory responsibilities?
Nurse Coordinator Clinical/ Samaritan Endoscopy
Three 12-hour shifts week (6:30a-7pm) with some required administrative call. Some holidays and weekends may be required.
Clinical Nurse Coordinator Jobs
By Central Vermont Medical Center At , Berlin, 05602, Vt $40.16 - $63.97 an hour

Building Name: CVMC - Central Vermont Medical Center Location Address: 130 Fisher Road, Berlin Vermont Regular Department: CVMC - Medical Surgical Full Time Standard Hours: 40 Shift: ...

Clinical Nurse Coordinator (Hybrid)
By EVERSANA At , Chesterfield, Mo
The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.
Perform patient/family education about disease state, management/plan of care, medication use and side effects, lifestyle and lifecycle considerations and resources
Provide overall clinical case management services to patients and caregivers, develop 1:1 relationships
Experience working with patients with chronic diseases in an education role
Delivery of superior nursing service and clinical education
Eligible for a hybrid work schedule (2 days/week remote) after first 90 days
Project Coordinator I (Clinical Study Associate)
By Labcorp At , Wilmington, 19805, De $25.75 - $35.00 an hour
Targeted skill development and/or growth of knowledge base.
Knowledge in global/regional regulatory and compliance requirements for clinical research.
Demonstrated excellence in task management and cross-functional collaboration.
Collaborate with Clinical Operations Manager, study teams, and Clinical Research Organizations
Perform developmental tasks as appropriate with oversight of CTA Manager.
Supporting additional ad-hoc activities as needed, as agreed with CTA Manager.
Clinical Study Coordinator - Plymouth, Ma
By Lightship At Plymouth, MA, United States
Required knowledge, skills, and abilities
Supporting supply and inventory management, including:
Updating the inventory management system
Bachelor's Degree in Life Science or healthcare-related field, or requisite combination of education, training, and experience
Understanding and complying with all regulations, policies, and guidelines applicable to clinical research, including GCP, FDA, and IRB requirements
Collecting study data and completing data entry / case report forms in various electronic systems and on paper
Clinical Study Manager Jobs
By ICON At , Remote
Supporting management of interactions with relevant line functions including data management, drug supply management, clinical development
Experience in proactive operational planning with effective contingency and risk mitigation plans
Development of specific sections of the protocol and related documents Development of study tools, guidelines and training materials
Ensuring trial information/results are reported within relevant trial repositories and tracking systems (e.g. trial results registries)
Timely, efficient and quality execution of assigned trials and trial related activities within budget, and in compliance with quality standards.
Nurse Iii-Clinical Coordinator Caps
By Health & Human Services Comm At , Austin, 78751, Tx $7,533 a month

Top 10 Tips for Success when Applying to Jobs at HHSC and DSHS

Clinical Study Coordinator Jobs
By Redbock - an NES Fircroft company At Dallas-Fort Worth Metroplex, United States
* Excellent written, verbal and interpersonal communication skills
* Strong organizational skills and attention to detail
* Proficiency in Spanish, phase II and/or phase III trial experience is a plus, but not required
* Communications and collaboration with patients, CROs, sponsors, PI(s) and internal teams, including participating in related meetings
* Support patient recruitment, ICF and CSR completion, protocol compliance, etc.
* Supply and equipment oversight
Clinical Study Project Manager
By Rangam At United States
Minimum of 3-5 years of project management experience in the pharmaceutical industry, with a focus on clinical study management
PMP or similar project management certification is preferred
Collaborate with cross-functional teams, including clinical operations, data management, biostatistics, and quality assurance, to ensure seamless study execution
Familiarity with Veeva or other relevant clinical trial management systems
Veeva or similar study management platform
Study Project Manager - 100% remote