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Clinical Trial Assistant Jobs

Senior Clinical Trial Assistant
By Theery At Redwood City, CA, United States
Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
Maintain and manage requests for access to and deactivation of study systems users.
Competency of the drug development process with knowledge of ICH-GCP is a plus
Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
Distribute safety alerts and relevant documents, if required
Maintain and update study team and vendor contact information
Clinical Trial Assistant - Oncology - Palo Alto, Ca
By ICON At , San Jose
Support clinical trial registration and disclosure on websites per applicable regulatory requirements
At least 1 year experience as a CTA, CRC, or other role in clinical trials.
Proven organizational and presentation skills
Ability to manage multiple tasks with meticulous attention to detail
Excellent written and verbal communication skills
Good knowledge of the ICH/GCP
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Assistant Jobs
By RemeGen Biosciences At Pennsylvania, United States
Assist with general response to patient enrollment inquiries and seek management support when needed.
Manage SVP and study team calendars and set up meetings.
Excellent written and verbal communication skills.
Strong attention to detail and problem-solving skills.
· 3+ years of experience in health care, biopharmaceutical experience is strongly preferred.
Assist the clinical development teams in completion of all required tasks to meet departmental and project goals.
Clinical Trial Research Assistant
By Durham Technical Community College At , , Nc $48,000 a year

% High School diploma or equivalent

Clinical Trial Assistant / Etmf (Electronic Trial Master File) Coordinator
By Krystal Biotech, Inc. At Pittsburgh, PA, United States
Knowledge of clinical research processes, regulatory requirements, and good clinical practice (GCP).
Familiarity with eTMF systems and other clinical trial management systems.
Liaise with project managers, clinical operations staff, and other relevant team members to facilitate document collection and retention.
Monitor the progress of clinical trials and report updates to the project manager or clinical team lead.
Previous experience in a similar role, preferably within a pharmaceutical or biotech environment.
Excellent organizational skills and attention to detail.
Clinical Trial Assistant - Milan
By DOCS At All, MO, United States

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, ...

Clinical Trial Assistant Jobs
By Precirix At Greater Boston, United States
·Expected educational qualifications: BSc or equivalent
·Minimum 2 years’ experience in with a clinical trial related role
·Experience with digital clinical trial systems such as eTMF, EDC, IRT etc
·Excellent communication skills (verbal, written and interpersonal) and negotiation skills
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Clinical Trial Assistant, Langen Hybrid
By DOCS At All, MO, United States
If you have a completed education in any ad
medical device and government and public health
ife science area (hotel, business a
Clinical Trial Assistant Jobs
By DOCS At All, MO, United States
Previous administrative experience preferably in the medical/ life science field.
Proven organizational and administrative skills.
Good knowledge of spoken and written Dutch and English.
• Contributes to the production and maintenance of study documents, en
Clinical Trial Assistant / Trial Documentation (Tmf)
By Apex Systems At United States
1. Provide start-up and ongoing trial regulatory document management
5. Setup and manage regulatory document trackers/reports as assigned.
6. Maintain a professional approach respecting the dignity and confidentiality of associates, manager, and vendors.
11. Maintain CEUs for SOCRA or ACRP certification.
• Oncology experience preferred. Prior experience managing flow of clinical trial regulatory documents preferred
4. Ensure quality product deliverables at all times.
Clinical Trial Assistant Jobs
By Cognito Therapeutics, Inc. At Cambridge, MA, United States
Assisting in the tracking, reporting and management of study metrics, lists, logs, lab samples, and licenses
Assist with vendor management, managing KPIs and recruitment metrics
Assist with DMC meeting management, preparation, and minutes
Manage study systems access requests, granting access to site staff where required
B.A./B.S. with 2+ years of relevant work experience
Good communication skills; team player
Clinical Trial Assistant-1 Jobs
By Cue Health At San Diego, CA, United States
Effective organizational and time management skills; ability to manage multiple assignments and changing priorities
Demonstrate commitment to the implementation and effectiveness of Cue’s Quality Management System
Knowledge of applicable clinical research regulatory requirements (e.g., GCP and ICH GCP)
Create, manage, and audit clinical trial master files and investigator site binders
A minimum of 1 year of experience in clinical research or related field
Previous experience in creating, managing, and auditing clinical trial master files and investigator site binders
Clinical Trial Assistant Jobs
By Cellenkos, Inc. At Houston, TX, United States
•Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
•Maintains current knowledge of FDA regulations, and GCP and ICH Guidelines for clinical research.
•Good written and verbal communication skills.
•To support the Clinical Operations teams with ongoing conduct of studies.
•To be familiar with ICH GCP, appropriate regulations, relevant SOP’s and internal tracking systems.
•To be familiar with the roles of the Clinical Research Associates (CRA) i
Research Assistant, Nida Clinical Trial - Temp To Perm - Bridgeport, Ct
By Orenco Systems, Inc. At Sutherlin, OR, United States
Strong organizational skills with experience using Microsoft Office software
Remote and in-office work; a skills test and strong portfolio are required.
Six years of related work experience
Bachelor's degree in a related field or Associate's Degree in a related field with related work experience
Experience collecting data using structured psychological assessments including administering assessments with substance using population
Experience and/or willingness to collect biological data regarding alcohol and drug use including urine, breath, and saliva samples collection
Research Assistant, Nida Clinical Trial - Temp To Perm - Bridgeport, Ct
By Liberation Programs, Inc. At Bridgeport, CT, United States
Strong organizational skills with experience using Microsoft Office software
Six years of related work experience
Bachelor's degree in a related field or Associate's Degree in a related field with related work experience
Experience collecting data using structured psychological assessments including administering assessments with substance using population
Experience and/or willingness to collect biological data regarding alcohol and drug use including urine, breath, and saliva samples collection
Record and compile information related to research data. Codes data accordingly to research specifications
Clinical Trial Assistant Jobs
By Corcept Therapeutics At Menlo Park, CA, United States
Assist project team with study specific documentation including filing to the Clinical Trial Management System and Trial Master File
Preferred Skills, Qualifications and Technical Proficiencies:
Track clinical supply inventory at sites and manage the site drug re-supply process
Set-up and maintain tracking system with oversight of manager
Develop working knowledge of company standard operating procedures (SOPs) and FDA regulations related to clinical studies
Familiarity with applicable regulatory requirements, Good Clinical Practice/ICH and Good Documentation Practices
Clinical Trial Assistant Project Manager | Mgh Cancer Center - Hybrid Remote
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Time management skills and ability to function effectively within a changing environment.
Provide first response for maintenance, personnel, and other research management issues.
Clinical Trial Assistant Project Manager | MGH Cancer Center - Hybrid Remote
Provides back-up coverage for the Clinical Trial Assistant Project Manager - CTTL Study Maintenance / Study Activation as applicable.
Manage special projects as assigned.
Demonstrated writing and editing skills.
Clinical Trial Assistant (Cta)
By Cytokinetics At , South San Francisco, 94080, Ca $31.50 - $38.50 an hour
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.
Clinical Trial Assistant (Cta)
By Cytokinetics At South San Francisco, CA, United States
Significant attention to detail, time management and organizational skills.
Support the clinical operations project teams under the supervision of Clinical Trial Managers.
BS/BA preferred; High school diploma or educational equivalent required.
Strong computer and software skills including proficiency in use of Microsoft Word, Excel, Outlook, Project, PowerPoint and Adobe Acrobat.
Excellent written and verbal communication skills.
May contact clinical trial sites, vendors, CROs, and partners as needed.

Are you looking for a rewarding career in clinical research? We are looking for a Clinical Trial Assistant to join our team and help us make a difference in the lives of patients. As a Clinical Trial Assistant, you will be responsible for coordinating and managing clinical trial activities, ensuring compliance with regulatory requirements, and providing administrative support. If you are passionate about clinical research and have excellent organizational and communication skills, this could be the perfect job for you!

Overview A Clinical Trial Assistant (CTA) is a professional who assists in the management of clinical trials. The CTA is responsible for providing administrative and operational support to the clinical trial team. This includes tasks such as data entry, tracking and filing documents, and coordinating with other departments. Detailed Job Description A Clinical Trial Assistant is responsible for providing administrative and operational support to the clinical trial team. This includes tasks such as data entry, tracking and filing documents, scheduling meetings, and coordinating with other departments. The CTA is also responsible for ensuring that all clinical trial documents are accurate and up-to-date. The CTA may also be responsible for preparing reports, tracking progress, and providing feedback to the clinical trial team. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite
• Knowledge of clinical trial processes and regulations
• Attention to detail
• Ability to multitask
• Ability to work under pressure
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical trials or research
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
Job Knowledge
• Knowledge of clinical trial processes and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of data management systems
Job Experience
• Previous experience in clinical trials or research
• Experience in data entry and data management
• Experience in preparing reports and tracking progress
Job Responsibilities
• Data entry and data management
• Tracking and filing documents
• Scheduling meetings
• Coordinating with other departments
• Preparing reports and tracking progress
• Ensuring accuracy and up-to-date clinical trial documents
• Providing feedback to the clinical trial team