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Clinical Trial Administrator Jobs

Clinical Trial Rater Jobs
By Wake Research At , Los Alamitos, Ca $70 - $90 an hour
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Intern - Cincinnati, Oh
By Medpace, Inc. At , Cincinnati, 45227, Oh
Excellent organizational, communication, and prioritization skills;
Knowledge of Microsoft Office; and
Competitive compensation and benefits package
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Provide day-to-day project support activities - maintenance of project-related files, corresponding with study teams, etc;
Perform administrative duties in conformity with company policies and procedures;
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
Clinical Trial Rater Jobs
By Wake Research At , Encino, Ca $70 - $90 an hour
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Clinical Trial Rater Jobs
By M3 USA At Los Angeles, CA, United States
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills
Strong written and verbal communication skills
This position offers a competitive salary of $70/hr - $90/hr.
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Senior Clinical Trial Manager
By Tourmaline Bio At United States
Strong working knowledge of cGCP/ ICH guidelines, and US and international clinical regulatory requirements
Develop and manage clinical trial budget and facilitate contract review
Adhere to relevant company policies and SOPs, cGCP/ICH guidelines, QC/QA procedures, as well as relevant clinical regulatory requirements
Advanced degree or certification is a plus
5+ years of clinical trial operations experience in a biotech, pharmaceutical, CRO, clinical research site or related healthcare company
Experience working on a multi-phase clinical program is a plus
Clinical Trial Manager Jobs
By Foresee Pharmaceuticals At Newark, DE, United States
·Contributes to the development and management of study specific agreements/budgets (i.e. non-disclosure agreements, clinical trial agreements, etc.)
·Analyzes data and clinical trial status against expectations and communicates potential risks and study progress to management.
·Manages Investigative Sites as needed via appropriate and consistent communication channels (e.g. telephone contact and e-mail).
·Complete other duties as assigned by manager.
·Excellent communication skills both written and spoken.
·Knowledge of and training in GCP/FDA/ICH regulations required.
Clinical Trial Manager Jobs
By Hays At Paramus, NJ, United States
Operations. The position is charged with independent site management of investigative sites, external
• Regular interaction with clinical management team and senior management
• Ability to effectively interact with and support all levels of management
Clinical Trial Manager – Permanent – Paramus, NJ. – $120,000 - $140,000
Our Client is seeking a Clinical Trial Manager in Paramus, NJ.
The Clinical Trial Manager is responsible for the day-to-day operations of clinical trials, clinical trial
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
Clinical Trial Transparency Medical Writer - Remote | Wfh
By Get It Recruit - Healthcare At Dedham, MA, United States

We are looking for a highly motivated and experienced Clinical Trial Transparency Specialist to join our dynamic team! As a Transparency Specialist, you will play a crucial role in ensuring that our ...

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 Rater Jobs
By Wake Research At , Tucson, Az
Solid teamwork, organizational, interpersonal, attention to detail, and problem-solving skills.
Strong written and verbal communication skills
Named in Fortune’s 2020 ‘Future 50’ list, ahead of Facebook and Amazon
Ranked in Forbes’ 2020 Global 2000 list of the world’s largest public companies
M3 is the only company incorporated after the year 2000 to be included in the Nikkei 225 Index
Listed in Forbes’ ‘Asia’s 200 Best Over a Billion’ in 2019
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
Global Clinical Trial Associate
By ICON Strategic Solutions At United States
Benefits of Working in ICON:
Organizes Study Team meetings and prepares meeting minutes
Assists with organizing Investigator Meetings
Assists with preparation and review of study documents
Ships study documents and supplies to investigational sites and tracks delivery
Submits study documentation to Trial Master File
Clinical Trial Coordinator Jobs
By BriaCell Therapeutics Corp. At Philadelphia, PA, United States

We seek a clinical trial coordinator who worked at a patient care level, to supervise sites remotely from the Sponsor's perspective.

Clinical Trial Associate Jobs
By X4 Life Sciences At Greater Boston, United States
Strong knowledge of MS Excel, dashboard building, task management
Previous experience in Clinical Trial Associate/Study Logistics Supply Manager capacity in industry or academic setting
Bachelor of Science in relevant discipline
Willingness to learn in a fast-paced, start-up biotech
Ability to work on a corp-to-corp basis under LLC
Furthermore, this company closed a Series A funding round in 2020, with total funding now exceeding $60M.
Clinical Trial Nurse - Orlando, Fl
By IQVIA At , Orlando, Fl
2+ years of IV infusion experience
Research/trial experience or experience in the field of cardiovascular (ICU, CCU, Cath Lab) would be a plus
Recent experience in drawing blood
Collecting samples and required information and data
IP preparation, administration, and post observation (1 hour)
Labelling and shipment of samples
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 an exciting opportunity to join a dynamic team of Clinical Trial Administrators? We are looking for a motivated individual to join our team and help manage our clinical trials. You will be responsible for ensuring that all clinical trial activities are conducted in accordance with applicable regulations and guidelines. If you have a passion for clinical research and are looking for a rewarding career, this could be the perfect job for you!

Overview A Clinical Trial Administrator is responsible for the administrative and operational aspects of clinical trials. This includes managing the trial budget, preparing and submitting regulatory documents, and coordinating the activities of the research team. The Clinical Trial Administrator is also responsible for ensuring that the trial is conducted in accordance with applicable laws and regulations. Detailed Job Description The Clinical Trial Administrator is responsible for the administrative and operational aspects of clinical trials. This includes managing the trial budget, preparing and submitting regulatory documents, coordinating the activities of the research team, and ensuring that the trial is conducted in accordance with applicable laws and regulations. The Clinical Trial Administrator is also responsible for ensuring that the trial is conducted in a timely manner and that all data is collected and reported accurately. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of clinical trial regulations and guidelines
• Ability to manage multiple tasks and prioritize workload
• Proficiency in Microsoft Office applications
• Knowledge of medical terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical trial administration
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of clinical trial regulations and guidelines
Job Knowledge
• Knowledge of clinical trial regulations and guidelines
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of clinical trial management systems
• Knowledge of data management systems
Job Experience
• At least two years of experience in clinical trial administration
• Experience in budget management
• Experience in preparing and submitting regulatory documents
• Experience in coordinating the activities of the research team
Job Responsibilities
• Manage the trial budget
• Prepare and submit regulatory documents
• Coordinate the activities of the research team
• Ensure that the trial is conducted in accordance with applicable laws and regulations
• Ensure that the trial is conducted in a timely manner
• Collect and report data accurately
• Monitor the progress of the trial
• Provide administrative support to the research team