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Clinical Trials Administrator Jobs

Clinical Trials Research Associate - Cancer Center
By University of Iowa At Iowa City, IA, United States
Minimum 1 year of clinical research experience or medical research data management experience.
Bachelor’s degree or an equivalent combination of education and experience.
Assists in the design, development, execution and administration of data entry for protocols and clinical studies.
Follows study participants; manages collection of data including maintaining records of patient visits/interviews.
Excellent verbal, written and interpersonal communication skills.
Ability to manage complex information with attention to detail and a high level of accuracy
Business Development Manager, Clinical Trials
By Clinitiative Health Research At Dallas, TX, United States
Ensure client satisfaction through continued relationship management
1+ years of experience in the clinical research industry, or similar 
Salesforce experience is a plus
Experience with clinical trials is a plus
A self-starter and a hunter’s mentality 
Bachelor's of Science, is a plus 
Clinical Trials Data Coordinator - Remote
By City of Hope At California, United States
Basic education, experience and skills required for consideration:
Data Management & Protocol Compliance
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Clinical Trials Data Coordinator - Remote
By City of Hope At Duarte, CA, United States
Basic education, experience and skills required for consideration:
Data Management & Protocol Compliance
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Project Leadership – Biotech (Clinical Trials) – Vaccine - Home Based
By Parexel At Durham, NC, United States

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, your ...

Clinical Trials Specialist Jobs
By Axle Informatics At Bethesda, MD, United States
Stay abreast of project management certification standards and industry principles through professional associations and implements practices. 4
Creates project in designated project management software and ensure all necessary staff have access.
Recommend and support routine project management meetings, updates and prepare a variety of status reports and dashboards.
Assist staff coordinate project management activities, to include routine meetings and development of reports.
Conducts project analysis and reports to upper management.
Develop summaries of project status and performance for review with upper management.
Clinical Trials Research Assistant - Cancer Center
By University of Iowa At Iowa City, IA, United States
Bachelor’s degree or an equivalent combination of education and experience
6 to 12 months experience in a research or health care setting
Excellent verbal, written and interpersonal communication skills
Ability to manage complex information with attention to detail and a high level of accuracy
Relevant experience in the conduct of clinical or laboratory research studies
Knowledge of regulatory guidelines and procedures
Clinical Trials Regulatory Specialist 1
By Stanford University School of Medicine At Stanford, CA, United States
Experience in clinical trials operations, knowledge of clinical trials regulatory requirements, or experience working with an IRB.
Knowledge, Skills And Abilities (required)
Bachelor’s degree and three years of related experience or a combination of education and relevant experience.
Manage and oversee new study initiation process, including educating study staff and sponsors, resolving issues and providing regulatory guidance and support.
Excellent communication skills and superb attention to detail.
Experience with MS Office products and database applications required.
Clinical Research Associate I - Clinical Trials Office
By Cedars-Sinai At West Hollywood, CA, United States
Participates in required training and education programs
1 year Clinical Research Related Experience preferred
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
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 Trials Coordinator Jobs
By Equiliem At Maryland, United States
Stay abreast of project management certification standards and industry principles through professional associations and implements practices.
Creates project in designated project management software and ensure all necessary staff have access.
Recommend and support routine project management meetings, updates and prepare a variety of status reports and dashboards.
Assist staff coordinate project management activities, to include routine meetings and development of reports.
Develop summaries of project status and performance for review with upper management.
Measure project performance using designated systems, tools and techniques and report findings to upper management.
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 Assistant I - Clinic
By Institute for Medical Research At Durham, NC, United States
Assist in the collection and management of clinical data and collection of source documents
Review CPRS (Computerized Patient Record System) patient charts to screen for possible subjects and to compile data
Perform tasks to ensure smooth clinic flow including organization of supplies, preparation of paperwork, and communication with study and clinical staff
Recruit and consent research participants for various clinical trials and research projects
Trouble-shoot and modify protocol implementation when necessary
Obtain various measurements from participants including vital signs and waist and hip circumference
Project Leadership - Biotech (Clinical Trials) - Rare Disease
By Parexel At Durham, NC, United States

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, your ...

Medical Writer Clinical Trials
By Hackensack Meridian Health At , Hackensack, 07601, Nj
Education, Knowledge, Skills and Abilities Required:
Education, Knowledge, Skills and Abilities Preferred:
Ensures potential study risks are escalated to management as appropriate.
Mandatory education on human subject research and GCP (CITI Training and Certification).
Excellent medical writing, communication, organizational, presentation, documentation, and interpersonal skills are required.
Possesses beginning to working knowledge of subject matter.
Clinical Trials Research Associate - Gastroenterology/Hepatology
By The University of Iowa At , Iowa City, Ia
Protocol Development/ Management and Study Responsibilities:
Excellent time management skills and the ability to perform detail oriented work independently is required
Experience with following specific protocol techniques and management is desirable.
Manage and organize regulatory documentation from sites and regulatory authorities.
Manage and organize regulatory documents from sponsors and CROs.
Excellent written and verbal communication skills are required.
Clinical Research Coordinator I - Clinical Trials
By Mount Sinai At , New York, 10029, Ny $58,661 - $80,000 a year
Candidate must have strong interpersonal communication skills, both written and verbal. Attention to detail and strong organizational skills are required.
One year clinical research experience preferred.
Track study coordinators specimen order supplies
Provide logistical support for ordering and tracking all study specimen supplies
Assemble specimen supply kits and ship them to the study sites
Will enter data into the electronic data capture system
Project Leadership - Clinical Trials -
By Parexel At , Remote

The Project Leadership function at Parexel is a critical part of driving success for our clients and advancing clinical research projects. As a part of the Global Project Leadership organization, ...

Clinical Research Nurse, Dahms Clinical Trials Unit - Part Time (24 Hours/Week)
By University Hospitals At , Cleveland, Oh
Demonstrates technical skills in care delivery that result in safe practice and positive care outcomes.
Implements the nursing process by delivering effective relationship based nursing care.
Demonstrates clear communication and effective collaboration to optimize patient care and clinical operations.
Develops self and contributes to the professional practice of nursing.
Displays leadership that influences optimal clinical and operational outcomes.
Diploma in Nursing, Associates in Science Degree in Nursing (ADN) or Master of Nursing from an accredited nursing program required.