Register
Recruit Create CV

Clinical Trials Navigator Jobs in Union, Arkansas

Remote Clinical Trials Manager - 210641
By Medix™ At United States
Possess a minimum of 7 years of clinical trial management experience, with a focus on recent Oncology trials.
Train team members and partners, maintain study files, provide regular updates to management, and ensure compliance with GCP.
Lead study teams, foster relationships with external partners (CROs, labs, IRBs, sites), and identify/manage risks.
Assist in site selection, create RFPs, negotiate contracts, manage budgets, and oversee invoicing.
Show experience in international trials and managing external providers, including CROs.
Efficiently oversee clinical trials, managing multiple studies within a development program.
Clinical Trials Associate - Neuroscience
By Worldwide Clinical Trials At United States
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Skill sets and proven performance equivalent to the
Maintain and quality audit to assure the most recent revisions of documents are on project portals
Clinical Trials Operations Specialist
By McInnis Inc. At United States
Desired Experience, Skills and Abilities:
Enter country level information in BI Clinical Trial Management System (CTMS) and related systems.
Under the direction of the CTL/CTM or Feasibility Manager (depending on the task/activity), the CTO will:
Create trial specific slide decks, training material, etc. in accordance with BI requirements.
Excellent communication skills (written and oral)
In addition to the CTO responsibilities and duties, they may provide assistance in leading the trial team:
Clinical Research Coordinator - Medicine Clinical Trials Office
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Trials Associate - Early Phase
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Clinical Care Navigator Jobs
By Lyra Health At United States
Significant experience managing high-risk clinical situations (e.g., suicidality, mandated reporting)
Continuing education support, including $1,000 annual stipend; plus coverage of standard licensure fees to maintain your license
Bilingual, Spanish-speaking candidates strongly preferred (but not required)
Must be a full time resident of the United States; work cannot be completed from outside the United States.
You must be able to work the following shift:
Monday-Friday 9:30 am-6:00 pm PT
Clinical Trials Associate- Oncology
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Clinical Trials Manager Jobs
By SPARK Neuro At United States
● Knowledge of clinical operations, project management tools and processes.
● Delegates and manages tasks and responsibilities to other team members assigned to the study
● In collaboration with data management, facilitates ongoing data review in preparation for interim,
judgment along with the ability to recommend business alternatives to senior management
This is a remote position with occasional travel.
● At least 6 years of clinical research experience including at least three (3) years having effectively
Oncore Compliance Analyst (Varying Levels - Remote), Clinical Trials
By University of Virginia At National, MD, United States
Experience working with a clinical trial management system (CTMS)
In addition to the above job responsibilities, other duties may be assigned.
Experience in clinical research and/or clinical compliance
Aid in executing compliance program components, including protocol review, record keeping, reporting, and evaluation.
Perform preliminary review of protocols and identify potential concerns, reporting them to supervisor.
Work with study teams to build calendars within research systems based on research protocols.
Clinical Trials Manager/Sr Clinical Trials Manager
By Medix™ At Gaithersburg, MD, United States
At least 5 years of clinical trial management experience; Recent Oncology trial
Effective trial management of a clinical study or multiple studies within a clinical
Management of the study team for assigned studies or programs and of relationships with
Provide management with routine updates regarding the status of ongoing studies
Understanding of cross-functional areas including data management / biostatistics,
Brochures, Study Manuals, Statistical Analysis Plans, CRFs, Data Management Plans, and
Project Associate (Remote), Clinical Trials Office
By University of Virginia At National, MD, United States
Experience with the following computer applications: OnCore, EPIC, Advarra EDC, other clinical trial management systems and electronic data capture system.
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Clinical Trials Nurse – Sarcoma Outpatient Setting, Nyc
By Memorial Sloan Kettering Cancer Center At , New York, 10017 $87,300 - $139,800 a year
Perform patient assessment, offer patient education and patient/family support
Three years clinical Nursing experience
Clinical research nursing experience preferred but not necessary
Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment
Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization.
Project Associate (Remote), Clinical Trials Office
By The Rector & Visitors of the University of Virginia At , $65,000 - $75,000 a year
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Knowledge of GCPs governing clinical research.
Senior Project Manager, Rwe Clinical Trials, Remote
By WALGREENS At , Deerfield, 60015 $143,460 - $196,010 a year
Bachelor’s degree in Life Sciences or related field and at least 4 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (ie. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
May manage a team as and when required
Identify changes in scope and manage the change control process, as necessary
Clinical Trials Research Nurse
By Premier Health At , Centerville, 45459, Oh
Current CPR certification required at the time of hire.
1 - 3 years of job-related experience
Effective interpersonal and communication skills
Must be able to multitask with constant interruptions while maintaining a pleasant demeanor.
CLINICAL TRIALS RESEARCH NURSE / RN
Full Time 8am-4:30pm / 80 Hours per Pay
Clinical Nurse Navigator Jobs
By BayCare At , Tampa, Fl
Does this position fall under CMS guidelines for COVID19 vaccine or exemption?: Yes - CMS Requirements Apply
Required - Bachelors - Nursing; Preferred - Masters - Nursing
Required - RN (Registered Nurse) - State of Florida; Required - Nurse Specialty - within 6 months
Location: St Josephs Main and Childrens
Status: Full Time, Exempt: Yes
Shift Hours: Varies - 8 hour shifts
Project Manager, Rwe Clinical Trials (Remote)
By Walgreens At Deerfield, IL, United States
Bachelor’s degree in Life Sciences or related field and at least 2 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (i.e. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
Identify changes in scope and manage the change control process, as necessary
Experience collaborating with others to deliver results to meet timeline, metrics and budget.
Clinical Trials Research Assistant - Pediatric Neonatology
By University of Iowa At Iowa City, IA, United States
Bachelor’s degree in a related field or an equivalent combination of education and/or related experience.
Communicates with Research Manager and PIs about the status of the research projects.
Communicates with Research Manager and PI about the status of the research projects.
Excellent written and verbal and interpersonal communication skills.
Ability to manage complex information with attention to detail and a high level of accuracy.
Six months to one year of experience in clinical research
Administrative Services Coordinator - Clinical Trials Unit
By Kennedy Krieger Institute At Baltimore, MD, United States
Schedule meetings as requested by the Manager of Medical Program Operations, faculty members, and CTU staff.
Develops, implements, and maintains efficient and effective systems for handling departmental administrative and clerical functions.
High School diploma or GED required.
AA or equivalent college-level program, business school degree, preferred.
Clinical Nurse Navigator Jobs
By Roper St. Francis Healthcare At Charleston, SC, United States

Job Summary The Clinical Nurse Navigator serves as a single point of contact for referring physicians, patients, and caregivers, enhancing communication among all. This job provides resources ...