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Clinical Trials Specialist 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 Specialist Rvt - Louisville
By Boston Scientific At Louisville, KY, United States
Maintain current Customer Relationship Management (CRM) records
A working knowledge of GMP, ISO 13485 & MDD requirements.
Assist or act as Field Mentor when asked in the training and educational needs of incoming field personnel.
Facilitate the adoption of Varithena through education and awareness with RVTs
3-5 years of experience in a healthcare field
3-5 years of experience in the medical device industry as a clinical specialist or equivalent
Clinical Specialist Jobs
By Outset Medical, Inc. At New York City Metropolitan Area, United States
Outset also offers the following benefits:
Effectively work cross-functionally with Outset Team members to deliver an exceptional customer experience.
Manage administrative tasks; reporting of dialysis treatments, training information and treatment growth outcomes in assigned region.
2 years of clinical experience, ideally in Dialysis
2 years medical device, biotech or pharmaceutical experience preferred
Excellent interpersonal skills with the ability to persuade decision makers
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 Specialist Jobs
By Planet Pharma At United States
Drive program adoption through ongoing clinician education, optimizing workflow, and delivering tangible results
2-5 years’ experience in the acute care healthcare setting
1-3 years’ medical device experience
Service, supply chain, or clinical experience perferred
MUST BE LOCATED IN CALIFORNIA, DENVER, CHICAGO, NYC, OR BOSTON
Engage hospital staff in customer business reviews, leveraging sustainability reports, savings metrics, and tracking to goals defined by the account
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.
Clin Trials Rsrch Asst/Data Mg
By University of Iowa At Iowa City, IA, United States
Protocol Development/Management And Study Responsibilities
Provide general assistance, as needed, to the PIC clinic and administrative managers, faculty and staff.
Excellent Written And Verbal Communication Skills Are Required.
Assist in the conduct of sponsored clinical trials, including the collection of clinical data and the compilation of results.
Assist in the design and development of data collection forms, questionnaires, and procedures manuals.
Design forms to facilitate the collection and tracking of study participant data, study drugs, biological specimens and study procedures.
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 Safeguarding Specialist Jobs
By Kooth USA At , Remote $70,000 - $80,000 a year
Contributes to the review of safeguarding processes, including risk management, risk reporting and risk prevention.
Ensures that any training regarding safeguarding and risk management is up to date with national and local policy.
Actively seeks to develop new skills through shadowing the training of others and continuous professional development opportunities.
Direct experience working within the youth behavioral health sector.
Excellent Medical, Dental and Vision benefits
Clinical Safeguarding Specialist | Full- Time, Remote
Clinical Specialist Jobs
By MedImpact Healthcare Systems At , Tempe, 85284, Az
Provide in-service education to PACs regarding topics such as PA guidelines, diagnoses commonly seen as part of the PA review process
Two (2) to five (5+) years related experience
Remote – Tempe, AZ or San Diego, CA
This job has no supervisory responsibilities.
To perform this job successfully, an individual should have knowledge of Microsoft Office Suite Word Processing software.
Responsible for providing clinical review support services to client plan(s) contracting for clinical services
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

Are you looking for a challenging and rewarding career in clinical trials? We are seeking a Clinical Trials Specialist to join our team and help us develop and execute clinical trials that will make a difference in the lives of patients. If you have a passion for clinical research and a commitment to excellence, this could be the perfect job for you!

Overview A Clinical Trials Specialist is a professional who is responsible for the coordination and management of clinical trials. They are responsible for ensuring that the clinical trial is conducted in accordance with the protocol and applicable regulations. They are also responsible for the collection and analysis of data, and for the preparation of reports and presentations. Detailed Job Description A Clinical Trials Specialist is responsible for the coordination and management of clinical trials. This includes the development of protocols, the selection and recruitment of study participants, the collection and analysis of data, and the preparation of reports and presentations. The Clinical Trials Specialist is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol and applicable regulations. Job Skills Required
• Knowledge of clinical trial protocols and regulations
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of data analysis and statistical methods
• Ability to manage multiple projects simultaneously
• Ability to work under pressure and meet deadlines
Job Qualifications
• Bachelor’s degree in a related field such as biology, chemistry, or health sciences
• Previous experience in clinical research or clinical trials
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of computer software programs such as Microsoft Office
Job Knowledge
• Knowledge of clinical trial protocols and regulations
• Knowledge of data analysis and statistical methods
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of computer software programs such as Microsoft Office
Job Experience
• Previous experience in clinical research or clinical trials
• Experience in project management
• Experience in data collection and analysis
Job Responsibilities
• Developing clinical trial protocols
• Recruiting and selecting study participants
• Collecting and analyzing data
• Preparing reports and presentations
• Ensuring that the clinical trial is conducted in accordance with the protocol and applicable regulations
• Maintaining accurate records of the clinical trial
• Monitoring the progress of the clinical trial