Clinical Study Manager - Ivd/Medtech - Remote
By NAMSA At United States
Act with integrity in everything we do.
Develop superior talent and deliver expertise.
Respond with agility and provide timely results.
Embrace collaboration, diverse perspectives and ideas.
Come and work for an organization with the:
Clinical Study Assistant Jobs
By Kelly Science, Engineering, Technology & Telecom At Irvine, CA, United States
Run reports including training matrix reports, metrics for management reviews
Support management of IRB/IEC renewal compliance.
Work with management group to help achieve department goals.
Requires experience and knowledge working with computer systems (Microsoft office –
Assist in payments/tracking for patient reimbursements. Performs data entry in systems
Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
Clinical Nurse Coordinator - Satellite Holding
By Synergy Global Technologies Inc. At Las Vegas, NV, United States
Education assistance (tuition, student loan, certification support, dependent scholarships)
Learn More About The Benefits Offered For This Job.
Family support through fertility and family building benefits with Progyny and adoption assistance.
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.
Collaborates with subject matter experts and other managers to create an environment of teamwork that supports improved outcomes and service.
Assists with staff scheduling. Manages all practical aspects of staff labor in accordance with patient care needs and established productivity guidelines.
Clinical Study Manager, Clinical Operations
By Daiichi Sankyo, Inc. At United States
Note that vendor management is not limited to the CRO, but includes ancillary vendors (e.g. translations, trial insurance, and central laboratory).
Ensure DS internal tracking systems are updated (e.g. Global Project Management System, GPMS).
Education Qualifications (from An Accredited College Or University)
Associate degree or with a nursing diploma with substantial experience preferred.
4 or More Years relevant experience is required with a BS preferred.
Bachelor's Degree in the Sciences preferred.
Clinical Research Coordinator - Maternal-Child Environmental Health Prospective Cohort Study
By Northwell Health At , New Hyde Park, 11042 $58,540 - $92,650 a year
Bachelor's Degree required, or equivalent combination of education and related experience.
Adheres to Good Clinical Practice, regulatory, and grant agency requirements
Collects, labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements
1-3 years of relevant experience, required.
Completes the activities assigned to the Clinical Research Coordinator by local research team and ECHO program leadership
Maintains comprehensive study documents/records as requested by ECHO program core elements, regulatory agencies, the NIH, and local study leadership
Study Coordinator Ii Jobs
By Cayuse Native Hawaiian Veterans, LLC At , Honolulu $30 - $35 an hour
Minimum 6 years or successful execution of over 30 clinical trial studies or collaborative biomedical laboratory study experience (Study Coordinator II)
Preferred experience in managing investigator-initiated, industry-sponsored, or military studies.
Ability to analyze data and summarize findings for incorporation into reports.
The Contractor shall match sponsored studies with appropriate Principal Investigator.
The Contractor shall assure that logs and collected data from patients enrolled in the study remain confidential.
Must have a Bachelors of Science in biomedical science field or nursing
International Clinical Nurse Coordinator
By Texas Children's Hospital At , Houston, 77001
BLS certification from the American Heart Association required
3 years' or more experience in nursing
Provides education concerning various aspects of the care
Coordinates initial education of patients by phone
RN License by Texas Board of Nursing or Nurse Licensure Compac
Responsible and accountable for the daily care coordination of patients within area of clinical
Clinical Study Nurse Coordinator
By University of Nebraska Medical Center At , Omaha $66,000 - $99,000 a year
Required Additional Knowledge, Skills and Abilities:
Preferred Additional Knowledge, Skills and Abilities:
If any experience is required, please specify what kind of experience:
If yes, what is the required licensure/certification?
Nursing experience in oncology and/or clinical research.
If yes, what is the preferred licensure/certification?:
Research Study Nurse Jobs
By Massachusetts General Hospital(MGH) At , Boston, 02114
Familiarity and comfort with Database management, Word, Access and Excel will be necessary to meet job needs
MA Licensure as an RN. Clinical research experience preferred;
Computer and Internet skills required;
Understanding of regulations and requirements related to nursing practice and research protocols;
The research nurse will have frequent telephone communication with subjects and must be skilled at communicating and obtaining necessary information;
Good interpersonal and communication skills;
Clinical Study Support - Icf
By ICON At , Remote
Bachelor’s Degree in business administration, finance, science or related field or equivalent experience.
Central Services Specialist - ICF Management
Co-manages maintenance of the centralized Informed Consent Form mailbox.
Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.
Experience in negotiating vendor contracts/budgets.
Proven ability to effectively manage change.
Sr Clinical Study Coordinator- Full Time -Cancer,Clinical & Translational Research
By Henry Ford Health At , Detroit
Analyzes protocol specific requirements and implements quality assurance measures to ensure physician, patient, and clinician compliance.
Three (3) years of related experience required.
Organizational, analytical, and problem-solving skills required.
Demonstrated verbal and written skills at professional level required.
CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP certification required.
education and training, the health system has trained nearly 40% of physicians currently practicing
Nurse Coordinator Clinical/Ukhc
By University of Kentucky At , Lexington $26.00 - $45.70 an hour
Skills / Knowledge / Abilities
Does this position have supervisory responsibilities?
Nurse Coordinator Clinical/ENT Service Line
Study Coordinator Jobs
By RootStaff At San Rafael, CA, United States
Relevant administrative experience including detail oriented, collaborative, positive attitude, ability to prioritize, proactive, and good follow up skills,
Administrative tasks and activities may be requested by a line manager, study team member, or GSO department staff.
Assist with tracking and review of Clinical Trial Insurance requirements, expiry dates, insurance renewal, certificate distribution, and archival
Activities and responsibilities may include:
The SS I is not allocated as a resource to any specific study or program.
BOARD Quarterly MVR GSO Compliance and other metrics
Assistant Study Coordinator Jobs
By MetroBoston Clinical Partners At Boston, MA, United States
currently conducting several trials and are seeking an experienced Assistant Study Coordinator.
Attending site qualification and initiation visits
280 Washington St, Suite 204
MetroBoston Clinical Partners is a growing research organization with two offices in the
metro Boston area. We have a friendly staff and a great work environment. We are
Assistant Study Coordinator part time
Time Rosewood Nature Study Area Education Coordinator
By Truckee Meadows Parks Foundation At Reno, NV, United States

Do you want to make a difference in your community? Are you ready to make an impact? Become an AmeriCorps member in Reno today at the Rosewood Nature Study Area with Truckee Meadows Parks Foundation! ...

Rosewood Nature Study Area Education Coordinator
By Truckee Meadows Parks Foundation At Reno, NV, United States

Do you want to make a difference in your community? Are you ready to make an impact? Become an AmeriCorps member in Reno today at the Rosewood Nature Study Area with Truckee Meadows Parks Foundation! ...

Clinical Nurse Coordinator Jobs
By Central Health Management At Overland Park, KS, United States
Two (2) years of clinical practice in the clinical specialty of his/her unit and leadership/ management experience is preferred
Collaborates with subject matter experts and other managers to create an environment of teamwork that supports improved outcomes and service.
Assists with staff scheduling. Manages all practical aspects of staff labor in accordance with patient care needs and established productivity guidelines.
BLS certification required and maintained.
What qualifications you will need:
Assists with admission and discharge processes to ensure efficient throughput and high quality, patient-centered care.
Study Coordinator Jobs
By Meet At United States
Oversee data collection, management, and entry into study databases, ensuring accuracy and completeness
Strong knowledge of clinical research processes, regulations, and guidelines.
Excellent organizational, communication, and interpersonal skills.
Collaborate with study teams to develop and implement study protocols, ensuring compliance with regulatory guidelines and ethical considerations
Coordinate participant recruitment and enrollment activities, including screening, selection, and informed consent processes
BA/BS degree in a relevant subject
Clinical Study Support- Icf
By ICON Strategic Solutions At United States
Co-manages maintenance of the centralized Informed Consent Form mailbox.
Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.
Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.
MUST CURRENTLY WORK AT A CRO/PHARMA
Reviews and validates quality and accuracy of Informed Consent Form templates.
Supports development of Informed Consent Form templates.
Associate Director Clinical Study Management
By BeiGene At United States
Management experience of CROs, Vendors and Consultants preferred
Ensures the competencies and skills required for the Clinical team is consistent with the company defined requirements
Mentor junior team members to support development by delegating responsibilities, overseeing and supporting development plans
8+ years progressive experience in clinical operations preferably within the biotech, pharmaceutical, and/or CRO environment
Possess understanding of treatment landscape, standard of care, upcoming approvals, and good knowledge of KOLs and investigators
Experience developing trial plans including site monitoring, pharmacy and lab manuals, risk mitigation strategies, trial budgets and site selection/feasibility as required