Clinical Trial Budget Negotiation Analyst - Remote
By UC San Diego Health At , San Diego $75,000 - $95,000 a year
Seven (7) years of related experience, education/training, OR a Bachelor’s degree in related area plus three (3) years of related experience/training.
Thorough knowledge of finance policies, practices, and systems.
Thorough knowledge and understanding of internal control practices and their impact on protecting University resources.
Demonstrated experience analyzing and drafting complex clinical trial budgets and negotiating mutually satisfying terms and conditions.
#122969 Clinical Trial Budget Negotiation Analyst - Remote
Candidates hired into this position may have the ability to work remotely.
Clinical Trial Assistant-1 Jobs
By Cue Health At San Diego, CA, United States
Effective organizational and time management skills; ability to manage multiple assignments and changing priorities
Demonstrate commitment to the implementation and effectiveness of Cue’s Quality Management System
Knowledge of applicable clinical research regulatory requirements (e.g., GCP and ICH GCP)
Create, manage, and audit clinical trial master files and investigator site binders
A minimum of 1 year of experience in clinical research or related field
Previous experience in creating, managing, and auditing clinical trial master files and investigator site binders
Clinical Trial Assistant Jobs
By Abbott Laboratories At , San Diego, Ca $24 - $49 an hour
To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
To provide general administrative support to the Clinical Affairs Department and assistance to department Manager(s) and Director(s).
Research or health care related academic or work experience preferable.
Good written and verbal communication skills.
To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.
Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
With supervision, assist in the accurate and appropriate study test article management.
Support the effective financial management of the clinical trial.
Other duties as assigned by appropriate management.
Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
Clinical Trial Manager Jobs
By Amgen At Thousand Oaks, CA, United States
Previous managerial experience directly managing people and/or experience in leading teams, projects, programs or directing the allocation of resources
High school diploma/GED and 12 years of Manufacturing & Operations experience OR
Associate’s degree and 10 years of Manufacturing & Operations experience OR
Bachelor’s degree and 5 years of Manufacturing & Operations experience OR
Master’s degree and 3 years of Manufacturing & Operations experience OR
Solid knowledge of downstream, as well as a general knowledge of the associated analytical and buffer preparation techniques
Clinical Trial Rater Jobs
By M3 USA At Los Alamitos, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Manager/Sr. Clinical Trial Manager
By Akero Therapeutics At San Francisco Bay Area, United States
Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
Experience as the regional lead for Europe, United States, and/or India.
Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
This position is for remote work, but may require domestic or international travel as required (valid travel documents must be obtainable).
At least 4+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
Clinical Trial Rater Jobs
By M3 USA At Los Angeles, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Assistant Jobs
By Corcept Therapeutics At Menlo Park, CA, United States
Assist project team with study specific documentation including filing to the Clinical Trial Management System and Trial Master File
Preferred Skills, Qualifications and Technical Proficiencies:
Track clinical supply inventory at sites and manage the site drug re-supply process
Set-up and maintain tracking system with oversight of manager
Develop working knowledge of company standard operating procedures (SOPs) and FDA regulations related to clinical studies
Familiarity with applicable regulatory requirements, Good Clinical Practice/ICH and Good Documentation Practices
Clinical Trial Assistant (Cta)
By Cytokinetics At , South San Francisco, 94080, Ca $31.50 - $38.50 an hour
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant (Cta)
By Cytokinetics At South San Francisco, CA, United States
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Manager Jobs
By 89bio At San Francisco, CA, United States
Experience in CRO selection and management including drafting request for proposals (RFPs), bidding process, etc.
Conduct Site Qualification Visits (SQVs) to assess investigator's staff, capabilities, and facilities
In-depth knowledge of FDA regulatory requirements and medical practice/techniques and terminology
Select and manage vendors (including CROs, central lab, etc.)
Manage investigational product supply at study and site levels
Work with Clinical Research Organizations (CROs) to ensure coordination of Sponsor and CRO responsibilities, obligations are being met
Clinical Trials Navigator Jobs
By UCLA Health At Los Angeles, CA, United States

Please see the link below for more information about this position! Reach out with any questions!

Clinical Nurse Navigator I - Neuroscience Administration
By Hoag Memorial Hospital Presbyterian At , Newport Beach, 92663, Ca $52.77 - $81.74 an hour
Neurosciences: Fulfills mandatory stroke education requirements per certification agency
Minimum of 5 years’ experience in nursing and 3 years’ of experience in area of specialty required.
Additional department specific requirements are as follows:
Registered Nurse in the State of California - Current and in good standing.
Neurosciences (Stroke): AANN (American Association of Neuroscience Nurses): SCRN or CNRN or ANVC (Association of Neurovascular Clinicians): NVRN-BC or ASC-BC
Salary Range: $52.7700 - $81.7400 /hour
Remote - Senior Clinical Trial Specialist
By Beacon Hill Staffing Group At United States
5+ years previous clinical research experience in clinical trial coordination, site management, and or vendor management.
Must have the ability to build and maintain positive relationships with management and peers
Manage the collection, review and approval of regulatory documents from clinical sites
Manages and tracks study specific payments
Manage ancillary vendors, such as a specialty lab
Review site visit reports, under the direction of the Clinical Program Manager or designee
Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
Clinical Trial Nurse Navigator
By The Leukemia & Lymphoma Society At Rye Brook, NY, United States
Use problem solving skills to help patients overcome obstacles to enrollment
Maintain/increase knowledge and understanding of hematologic cancers, blood and bone marrow transplant and psychosocial aspects of living with cancer
Outstanding critical thinking, problem-solving, and collaboration skills
Demonstrated commitment to independent learning and skill enhancement
Serve in consulting role to the Information Resource Center about clinical trials
Contribute to continual process improvement of clinical trial support procedures
Clinical Trial Nurse - Nyc, Ny
By IQVIA At , New York $67,000 - $83,200 a year
2+ years of peds experience
Recent experience in drawing blood
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Collecting samples and required information and data
IP preparation, administration, and post observation (1 hour)
Labelling and shipment of samples
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Assistant Jobs
By RemeGen Biosciences At Pennsylvania, United States
Assist with general response to patient enrollment inquiries and seek management support when needed.
Manage SVP and study team calendars and set up meetings.
Excellent written and verbal communication skills.
Strong attention to detail and problem-solving skills.
· 3+ years of experience in health care, biopharmaceutical experience is strongly preferred.
Assist the clinical development teams in completion of all required tasks to meet departmental and project goals.
Clinical Trial Coverage Analyst, Remote
By University of Maryland Medical System At Baltimore, MD, United States
Skill in cost/financial accounting and clinical trial management software.
IV. Knowledge, Skills, And Abilities
Bachelor’s degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting, Nursing, or a related field required.
Certification in Healthcare Research Compliance or Epic preferred.
Demonstrated skill tracking clinical and corporate contracts using electronic administration software such as Grant.gov, CICERO, OnCore, Epic, etc.
Creates coverage analysis grids and analyzes the performance of the actual coverage analysis.
Director, Clinical Trial Recruitment
By Spectrum Science - a GHMC Company At New York City Metropolitan Area, United States
Meets deadlines, manages priorities and effectively communicates to team members, vendor partners and supervisors.
At least 5-7 years of clinical trial patient recruitment and retention experience working in a global clinical trial environment
Advanced knowledge of Microsoft Office (Outlook, PowerPoint, Word, etc.)
Excellent written and verbal communication skills; strong presentation skills
If you choose to go into an office, take advantage of the pre-tax transportation benefits.
If you choose to work from home, use the office equipment stipend.
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
Clinical Trial Intern - Dallas, Tx
By Medpace, Inc. At , Irving, 75038, Tx
Excellent organizational, communication, and prioritization skills;
Knowledge of Microsoft Office; and
Competitive compensation and benefits package
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc;
Perform administrative duties in conformity with company policies and procedures;
Clinical Trial Research Assistant
By Durham Technical Community College At , , Nc $48,000 a year

% High School diploma or equivalent

Clinical Trial Coordinator (Cqm) - Home-Based
By ICON At , Remote
B.S. or Advanced Degree (or equivalent degree/experience in the opinion of the Hiring Manager)
Manages the collection and retention of training signature logs
Minimum of 1-4 years of relevant work experience
Strong communication (written and verbal) skills to be able to interact with internal Vertex groups as well as external groups
Demonstrates a working knowledge of ICH GCP regulations and clinical protocols
Distributes SUSAR reports to investigators
Clinical Trial Analyst Jobs
By Randstad Life Sciences US At Cambridge, MA, United States
Supporting additional ad-hoc activities as needed, as agreed with CTA Manager.
Maintaining knowledge of systems and processes.
Perform departmental tasks as needed.
Review and/or approval of study documentation, including essential document packets, study plans, informed consent forms, etc.
Supporting oversight of risk-based monitoring.
Attendance of key team meetings as required; may make presentations (e.g. data, etc.).
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 ...

Clinical Navigator - Rn (Texas - Fully Remote)
By MicroTransponder At Dallas, TX, United States
Prior experience in the office or hospital setting, patient education and coordination of care is a MUST
Prior experience in the office or hospital setting, patient education and coordination of care
Provide education on Vivistim through immediate phone education where appropriate and/or scheduling for field education when needed.
Perform initial virtual education for Vivistim Paired VNS therapy
Manage related patient information in CRM system. Maintains updates/plan of action for patients desiring Vivistim based on interactions
Proficiency with Word, Excel, PowerPoint, Gmail, database programs and excellent typing skills are a MUST
Clinical Trial Assistant / Etmf (Electronic Trial Master File) Coordinator
By Krystal Biotech, Inc. At Pittsburgh, PA, United States
Knowledge of clinical research processes, regulatory requirements, and good clinical practice (GCP).
Familiarity with eTMF systems and other clinical trial management systems.
Liaise with project managers, clinical operations staff, and other relevant team members to facilitate document collection and retention.
Monitor the progress of clinical trials and report updates to the project manager or clinical team lead.
Previous experience in a similar role, preferably within a pharmaceutical or biotech environment.
Excellent organizational skills and attention to detail.
Clinical Trial Monitoring Specialist
By Infosoft, Inc. At United States
3-5 years of experience required
Experience with medical device monitoring is required.
Experience with cardiac trials and/or blinded trials is preferred.
Experience with Medidata RAVE and Medidata CTMS is preferred.
Remote with frequent travel to clinical sites (Pacific or Mountain Time Zone)
remote and onsite monitoring activities

Are you looking for an exciting opportunity to make a difference in the lives of patients? Join our team as a Clinical Trial Navigator and help us make a positive impact on the lives of those we serve! As a Clinical Trial Navigator, you will be responsible for providing support and guidance to patients and families throughout the clinical trial process. You will be the go-to person for all questions and concerns related to the trial, and you will ensure that patients are informed and comfortable throughout the process. If you are passionate about helping others and have a strong background in clinical research, this is the perfect job for you!

Overview Clinical Trial Navigators are responsible for providing support and guidance to patients and their families throughout the clinical trial process. They are responsible for helping patients understand the clinical trial process, providing information about the trial, and helping them navigate the various steps of the trial. They also provide support to the clinical trial team by helping to coordinate patient visits, providing patient education, and helping to ensure that the trial is conducted in accordance with the protocol. Detailed Job Description Clinical Trial Navigators are responsible for providing support and guidance to patients and their families throughout the clinical trial process. They are responsible for helping patients understand the clinical trial process, providing information about the trial, and helping them navigate the various steps of the trial. They also provide support to the clinical trial team by helping to coordinate patient visits, providing patient education, and helping to ensure that the trial is conducted in accordance with the protocol. They must be able to communicate effectively with patients, families, and clinical trial staff, and must be able to explain complex medical information in a way that is easy to understand. Clinical Trial Navigators must also be able to work independently and as part of a team. Job Skills Required
• Excellent communication and interpersonal skills
• Ability to explain complex medical information in an easy to understand manner
• Ability to work independently and as part of a team
• Knowledge of clinical trial protocols and procedures
• Knowledge of medical terminology and medical records
• Ability to coordinate patient visits and provide patient education
• Ability to maintain patient confidentiality
• Ability to work with a variety of people from different backgrounds
Job Qualifications
• Bachelor’s degree in a related field such as nursing, health sciences, or social work
• Previous experience in a clinical setting
• Knowledge of clinical trial protocols and procedures
• Knowledge of medical terminology and medical records
• Ability to coordinate patient visits and provide patient education
• Ability to maintain patient confidentiality
• Ability to work with a variety of people from different backgrounds
Job Knowledge
• Knowledge of clinical trial protocols and procedures
• Knowledge of medical terminology and medical records
• Knowledge of patient privacy laws and regulations
• Knowledge of patient rights and responsibilities
• Knowledge of clinical research and clinical trial processes
• Knowledge of patient education and support services
Job Experience
• Previous experience in a clinical setting
• Previous experience working with patients and families
• Previous experience working with clinical trial