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Clinical Study Coordinator Jobs

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.
Research Study Coordinator Jobs
By University of Washington At Seattle, WA, United States
Demonstrated experience in grant preparation, contract management, and IRB protocol development/adherence;
Strong organizational and time management skills with ability to lead research projects;
A Bachelor's degree in a relevant academic area AND two years of experience as a Research Study Coordinator DESIRED QUALIFICATIONS
Other miscellaneous administrative support. MINIMUM REQUIREMENTS
Experience in the preparation of academic manuscripts, posters, and presentations;
Excellent verbal and written communication skills including the ability to communicate via email effectively and efficiently; the ability to work independently;
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
Program Coordinator (Sports & Bible Study Missionary)
By Catholic Sports At , $25,000 - $69,000 a year
Management and leadership development, including opportunities to advance in Catholic Sports
Missionaries will also be offered benefits, not limited to, but such as:
15% managing volunteer league managers and visiting their leagues, or running leagues in the absence of volunteers
Interpersonal skills are critical for this role: Being invitational and outgoing towards participants, especially the newcomers
Computer/technical skills (Google products, Microsoft Office, Windows and social media marketing
25% leading the Bible study regional effort, including leading their own Bible studies & one-on-one outreach/discipleship
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
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?:
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
Clinical Study Manager- Medical Devices
By Integrated Resources, Inc ( IRI ) At United States
Remote will be considered; however, Minnesota or central time zone will be preferred.
Familiarity with electrophysiology and/or cardiac arrhythmias is a plus.
Previous work history with CERs and EU MDRs
Previous work history in medical device or pharmaceutical research (i.e., no academia or research scientist candidate).
Previous work history in the cardiovascular space.
Minimum is BS + proven work history
Rn Study Coordinator - Bsn
By Mayo Clinic At , Scottsdale, 85259 $79,747 - $119,683 a year

Affirmative Action and Equal Opportunity Employer

Research Study Coordinator - Temporary
By Texas State University At , San Marcos, 78666 $20 - $25 an hour
Knowledge of physiology; conduct of research; & proper patient interaction skills.
Skilled in: data entry, specimen collection, processing, storage, and analysis; & operation of PC-based programs.
Attend and participate in research symposia and continuing education as requested by the manager.
Maintain source documents and patient education materials for clinical trials.
Job duties under the direction of the principal investigator:
This is a Non-Benefits Eligible Part-Time (less than 20 hrs/wk) position.
Behavior Technician (Research Study Coordinator 1)
By University of Washington At , Seattle, 98195 $3,318 - $4,409 a month
Bachelor’s degree in related field (psychology, education, human/child development).
Experience working directly with children and families with Autism Spectrum Disorders.
As a UW employee, you will enjoy generous benefits and work/life programs.
To accurately record client intervention data and manage records.
Implement intervention protocols developed by BCBA to increase skills/reduce problem behaviors.
Certified Behavior Technician (CBT) credential in the state of Washington through the DOH.
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! ...

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.

Are you looking for an exciting opportunity to be part of a dynamic clinical research team? We are seeking a Clinical Study Coordinator to join our team and help us make a difference in the lives of patients. As a Clinical Study Coordinator, you will be responsible for managing clinical studies from start to finish, ensuring that all study protocols are followed and that data is collected and reported accurately. If you are a detail-oriented individual with excellent organizational skills, this could be the perfect job for you!

Overview Clinical Study Coordinators are responsible for managing the day-to-day operations of clinical research studies. They are responsible for ensuring that all study protocols are followed, that data is collected accurately, and that the study is conducted in compliance with all applicable regulations. Detailed Job Description Clinical Study Coordinators are responsible for the overall management of clinical research studies. This includes developing and implementing study protocols, recruiting and enrolling study participants, collecting and managing study data, and ensuring that all study activities are conducted in compliance with applicable regulations. Clinical Study Coordinators also provide support to the study team, including physicians, nurses, and other healthcare professionals. Job Skills Required
• Strong organizational and communication skills
• Knowledge of clinical research protocols and regulations
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office and other computer applications
• Ability to manage multiple tasks and prioritize work
• Attention to detail
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical research or healthcare
• Certification in clinical research (e.g., CCRC, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of data management systems
Job Experience
• Previous experience in clinical research or healthcare
• Experience in data collection and management
• Experience in recruiting and enrolling study participants
Job Responsibilities
• Develop and implement study protocols
• Recruit and enroll study participants
• Collect and manage study data
• Ensure compliance with applicable regulations
• Provide support to the study team
• Monitor study progress and report any issues
• Prepare study reports and presentations