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Junior Clinical Trials Data Specialist Jobs

Clinical Data Specialist Jobs
By Intellectt Inc At Alameda, CA, United States
At Least 3 years of experience in clinical data management and computer savvy. Some project management skills are needed.
Clinical data management experience needed.
They must be open to do menial tasks if they have 5 years experience.
Hybrid role (4 days onsite and 1 day remote)
A team player and flexible; quick and eager to enter into ADC.
Product: a sensor that will b put on the patient
Data Scientist, Rwe Clinical Trials, Remote
By Walgreens At Deerfield, IL, United States
Bachelor's degree or graduate degree and at least 4 years of experience in a quantitative or computational function
4 years of experience in R, Python, or SQL.
Experience in designing and executing robust and reproducible statistical analyses in the context of epidemiology and observational research with healthcare data
Experience processing large data from various data sources
Experience handling protected patient health information
Knowledge of at least one of the following: Tableau, Power Bi, Alteryx, Spotfire, or other BI intelligence tools
Research Data Assistant - Clinical Trials (Full Time, Day Shift)
By Nicklaus Children's Hospital At , Miami, 33155
High School education or equivalent
Assists study staff with any concerns or questions by promptly providing the information and feedback as requested
Enters data in databases, generates reports, performs data/database maintenance, performs data tracking, and performs queries.
Provides auditable trail of documentation with consistency among data base, records and required reports
Provides reports on grant progress and assists in troubleshooting
Serves as liaison for Research Institute with all departments involved with the study.
Clinical Trials Operations Specialist
By McInnis Inc. At United States
Desired Experience, Skills and Abilities:
Enter country level information in BI Clinical Trial Management System (CTMS) and related systems.
Under the direction of the CTL/CTM or Feasibility Manager (depending on the task/activity), the CTO will:
Create trial specific slide decks, training material, etc. in accordance with BI requirements.
Excellent communication skills (written and oral)
In addition to the CTO responsibilities and duties, they may provide assistance in leading the trial team:
Clinical Trials Specialist Jobs
By Vitalief Inc. At New Brunswick, NJ, United States
Needs to be communicative and responsive and know when to escalate and communicate issues to management.
Oncology clinical research experience is required.
Any experience working with solid tumors is a big plus.
Demonstrated computer skills with Microsoft Office applications.
Vitalief is offering a $3,500 sign-on bonus for this position!
You'll impact clinical research in various therapeutic areas, including oncology, and improve outcomes for diverse populations.
Travel & Trials Event Specialist
By Kirkland & Ellis At Los Angeles, CA, United States
Manage and effectively communicate Firm’s travel needs to vendors/resources.
Work on developing internal processes to enhance travel experience for attorneys and staff.
A minimum of 5 years of experience in travel or hotel sales and a Bachelor’s Degree.
Establishment and promotion of strong working relationships with external contacts and suppliers to ensure the Firm’s needs are understood and met.
Creation and dissemination of travel resource communication to the Firm.
Develop relationships with paralegals to assist with their trial related travel needs including contracting hotel guest room and meeting space.
Clinical Trials Data Specialist
By Stanford University School of Medicine At Stanford, CA, United States
Knowledge, Skills And Abilities (required)
Experience with Electronic Data Capture (EDC)
Some knowledge of medical terminology
Strong clerical, interpersonal, and organizational skills.
Ability to exercise judgment and employ basic reasoning skills.
Extraction and entry of required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs).
Clinical Data Specialist Jobs
By Merative At United States
Pharmacy technician certification plus 2 years related work experience, or 4 years related work experience.
Demonstrated ability to effectively communicate with management and other team members
Demonstrated ability to apply pharmacy knowledge and experience in critical thinking and problem solving; ability to recognize discrepancies in data
Perform data normalization prior to data entry, using controlled terminology and following strict editorial guidelines
Strong computer skills; familiarity with Microsoft Office products (e.g., Word, Excel, Access) and Adobe Professional
Solid knowledge of internet searching and pharmaceutical terminology
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.
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 Data Management Specialist
By TalentBurst, an Inc 5000 company At Irvine, CA, United States
Proven track record or validating, testing, and meeting reoccurring deadlines regarding data management.
Position: Analyst, Clinical Data Management
2-4 years of experience required.
Experience with EDC (Electronic Data Capture) systems required.
Good computer skills in Microsoft Office Suite
Good written and verbal communication skills and interpersonal relationship skills
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 Specialist (Multiple Vacancies)
By Rutgers University At New Brunswick, NJ, United States
Equivalent education, experience and/or training may be substituted for the educational requirement.
Minimum of three (3) years of clinical research experience.
At least one (1) year of oncology experience.
Bilingual skills (English/Spanish); speaking, reading, and writing.
Collaborates with Protocol Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list.
Serves as an essential link between patients and all other members of the research team.
Clinical Trials Data Entry Specialist
By UCLA Health At , Los Angeles, 90095, Ca $24.28 - $48.04 an hour

Description As the Data Entry Specialist, you will participate in all research activities as part of the clinical research team located at UCLA/UCLA Santa Monica while under the direction of the ...

Clinical Trials Disclosure Specialist
By Synectics Inc. At New Jersey, United States
Project and stakeholder management experience
US military experience will be considered towards industry experience requirements
2-3 years of document redaction and 5 years relevant work experience in a scientific or medical field with BA/BS
Exceptional written and oral communication skills
Strong organizational skills with the ability to multitask and prioritize
BA/BS or MA/MS in scientific or medical field
Clinical Trials Data Coordinator (Remote)
By City of Hope At California, United States
Basic education, experience, and skills required for consideration:
Preferred education, experience, and skills:
City of Hope’s commitment to Diversity, Equity, and Inclusion
Clinical Trials Administrator Jobs
By Weill Cornell Medicine At , New York, 10065, Ny $86,200 - $110,600 a year
Experience with regulatory, data management, and billing compliance aspects of clinical research.
Approximately 3 years of experience in health-related role, in clinical or research setting.
Experience with conducting and carrying out protocols and research coordination.
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Serves as liaison with the Food and Drug Administration (FDA), as indicated, to obtain Investigational New Drug (IND) number or exemption.
Assists leadership with developing and implementing strategies to build and grow the program's clinical research portfolio.
Clinical Trials Nurse Ii - Cts
By Memorial Sloan Kettering Cancer Center At , New York, 10017, Ny $87,300 - $139,800 a year
Perform patient assessment, offer patient education and patient/family support
A minimum of 2-5 years of oncology nursing experience required
Clinical research nursing experience highly preferred
Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment.
Committed and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and passion.
A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization.
Clinical Data Specialist Jobs
By Stanford University At , Stanford, Ca $68,000 - $82,000 a year
KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
High school diploma, G.E.D., or equivalent and three years of relevant experience or a combination of education and relevant experience.
Clinical knowledge in the field of oncology or blood and marrow transplantation
Basic knowledge of medical terminology
Excellent mathematical and analytical skills
Excellent communication skills, ability to relate effectively in person and work well in a team

Are you looking for an exciting opportunity to join a fast-paced clinical trials team? We are looking for a Junior Clinical Trials Data Specialist to join our team and help us manage and analyze data from clinical trials. This is a great opportunity to gain experience in a fast-growing field and make a real impact on patient care. If you're ready to take on a challenge and make a difference, apply now!

Overview A Junior Clinical Trials Data Specialist is responsible for collecting, organizing, and analyzing clinical trial data. They are responsible for ensuring that all data is accurate and up-to-date, and that it meets the standards of the clinical trial. They also provide support to clinical trial teams and other stakeholders in the clinical trial process. Detailed Job Description A Junior Clinical Trials Data Specialist is responsible for collecting, organizing, and analyzing clinical trial data. They are responsible for ensuring that all data is accurate and up-to-date, and that it meets the standards of the clinical trial. They also provide support to clinical trial teams and other stakeholders in the clinical trial process. This includes creating and maintaining databases, preparing reports, and providing technical assistance. They must also be able to identify and resolve data discrepancies. Job Skills Required
• Knowledge of clinical trial processes and regulations
• Proficiency in data analysis and interpretation
• Ability to work with large datasets
• Excellent organizational and communication skills
• Attention to detail
• Ability to work independently and as part of a team
• Knowledge of database management systems
Job Qualifications
• Bachelor’s degree in a related field
• Experience in clinical trials data management
• Knowledge of clinical trial processes and regulations
• Proficiency in data analysis and interpretation
• Ability to work with large datasets
• Excellent organizational and communication skills
• Attention to detail
• Ability to work independently and as part of a team
• Knowledge of database management systems
Job Knowledge
• Knowledge of clinical trial processes and regulations
• Knowledge of database management systems
• Knowledge of data analysis and interpretation
• Knowledge of clinical trial data management
Job Experience
• Experience in clinical trials data management
• Experience in data analysis and interpretation
• Experience in database management systems
• Experience in working with large datasets
Job Responsibilities
• Collect, organize, and analyze clinical trial data
• Ensure accuracy and up-to-date data
• Create and maintain databases
• Prepare reports
• Provide technical assistance
• Identify and resolve data discrepancies
• Support clinical trial teams and other stakeholders in the clinical trial process