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Clinical Trial Administrator Jobs

Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
Clinical Trial Nurse - Nyc, Ny
By IQVIA At , New York $67,000 - $83,200 a year
2+ years of peds experience
Recent experience in drawing blood
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Collecting samples and required information and data
IP preparation, administration, and post observation (1 hour)
Labelling and shipment of samples
Director, Clinical Trial Recruitment
By Spectrum Science - a GHMC Company At New York City Metropolitan Area, United States
Meets deadlines, manages priorities and effectively communicates to team members, vendor partners and supervisors.
At least 5-7 years of clinical trial patient recruitment and retention experience working in a global clinical trial environment
Advanced knowledge of Microsoft Office (Outlook, PowerPoint, Word, etc.)
Excellent written and verbal communication skills; strong presentation skills
If you choose to go into an office, take advantage of the pre-tax transportation benefits.
If you choose to work from home, use the office equipment stipend.
Clinical Trial Analyst Jobs
By Randstad Life Sciences US At Cambridge, MA, United States
Supporting additional ad-hoc activities as needed, as agreed with CTA Manager.
Maintaining knowledge of systems and processes.
Perform departmental tasks as needed.
Review and/or approval of study documentation, including essential document packets, study plans, informed consent forms, etc.
Supporting oversight of risk-based monitoring.
Attendance of key team meetings as required; may make presentations (e.g. data, etc.).
Clinical Administrator Jobs
By The Judge Group At North Carolina, United States
-Assigns and reassigns members to appropriate Care Manager under the direction of the Care Management Supervisor
-Assists with administrative/enrollment activities for special programs e.g., disease management, complex case management, behavioral health referrals
-Documents all member related activities in care management platform
-Utilizes plan software to generate care management reports
Remote, but most be located in North Carolina
-Communicates member Inpatient status to the assigned Care Manager
Clinical Trial Monitoring Specialist
By Infosoft, Inc. At United States
3-5 years of experience required
Experience with medical device monitoring is required.
Experience with cardiac trials and/or blinded trials is preferred.
Experience with Medidata RAVE and Medidata CTMS is preferred.
Remote with frequent travel to clinical sites (Pacific or Mountain Time Zone)
remote and onsite monitoring activities
Clinical Trial Administrator-1 Jobs
By PharmiWeb.Jobs: Global Life Science Jobs At South Carolina, United States
Note - Specific skills and experience requirements may vary depending on the Country
Performs data entry into various databases/applications
Manages meetings/logistics, payments, and document archives
Undergraduate degree or relevant experience - at the discretion of the CRD
1 year experience in relevant administration (depending on the tasks required).
Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt
Clinical Trial Administrator Ii
By PSI CRO AG At Durham, NC, United States
Be responsible for document management
College/University degree or an equivalent combination of education, training & experience
Administrative work experience, preferably in an international setting
Prior experience in Clinical Research
Be the point of contact for investigational sites, vendors, and multi-functional project teams
Update and maintain (automated) tracking systems and schedules
Clinical Trial Manager Jobs
By Amgen At Thousand Oaks, CA, United States
Previous managerial experience directly managing people and/or experience in leading teams, projects, programs or directing the allocation of resources
High school diploma/GED and 12 years of Manufacturing & Operations experience OR
Associate’s degree and 10 years of Manufacturing & Operations experience OR
Bachelor’s degree and 5 years of Manufacturing & Operations experience OR
Master’s degree and 3 years of Manufacturing & Operations experience OR
Solid knowledge of downstream, as well as a general knowledge of the associated analytical and buffer preparation techniques
Clinical Trial Manager Jobs
By NewAgeSys, Inc At New Jersey, United States
Leadership and Influence: Candidate's skills and capabilities in addressing complex situations, resolving conflicts, horizontal and vertical influencing.
Req Title: Clinical Trial Manager
Work Address: 900 Ridgebury RD BLDG AOB,, Remote, Remote
Leads the local trial team as an OPU Clinical Trial Manager (CTM) Trial Preparation, Conduct and Closeout:
Strong communication skills in complex cross-functional matrix structures.
Highly developed receptive communication skills and cultural sensitivity.
Clinical Trial Educator Jobs
By IQVIA At , Remote
Some roles require direct interaction with patients to offer education on trial, disease, and/or device/medication
Provides education to health care professionals and their staff, reinforces study protocols as related to a clinical trial
Maintains up-to-date technical knowledge of specialty and disease areas
Bachelor's Degree BA/BS in Health Sciences or related field or equivalent academic professional qualifications. Req
Typically requires 1 - 2 years of prior relevant experience. Req
Excellent interpersonal and communication skills
Clinical Trial Manager Jobs
By Astrix At United States
Strong project management and team leadership capability
Leads local trial team to ensure integrity of trial conduct, assurance of patient safety, in line with regulatory requirements
Leads the local trial team as an OPU Clinical Trial Manager (CTM) Trial Preparation, Conduct and Closeout
B.S., M.S., or PhD plus a minimum of 3 years of experience in clinical research in pharmaceutical industry
Knowledgeable across all aspects of clinical trial operations and execution.
In collaboration with Site Monitoring Lead and CRAs, ensure Trial contact for CRAs, investigators and site staff.
Clinical Trial Educator – Pediatric Cardiology – Nationwide – Hab80850
By IQVIA At , Remote
Some roles require direct interaction with patients to offer education on trial, disease, and/or device/medication
Provides education to health care professionals and their staff, reinforces study protocols as related to a clinical trial
Maintains up-to-date technical knowledge of specialty and disease areas
Bachelor's Degree BA/BS in Health Sciences or related field or equivalent academic professional qualifications. Req
Clinical Research Experience. 2 yrs Req
Excellent interpersonal and communication skills
Clinical Trial Manager - Remote
By Maxis Clinical Sciences At Ridgefield, CT, United States
Solid project management, networking/stakeholder management and team leadership capability
Candidate's skills and capabilities in addressing complex situations, resolving conflicts, horizontal and vertical influencing.
Candidate's skills and capabilities in setting priorities, managing pace of activities, and efficient usage of resources.
Job Title: Clinical Trial Manager
Duties:As Clinical Trial Manager (CTM)
Leads the local trial team as the US Clinical Trial Manager (CTM) Trial Preparation, Conduct and Closeout:
Clinical Trial Document Management (Ctdm) Specialist
By Alcon At United States
Enter and maintain site information and document tracking in current clinical trial management systems.
Travel Requirements: minimal to no travel if located in Fort Worth; less than 10% if remote
Bachelor’s Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)
Basic knowledge of clinical trial processes
Alcon provides a robust benefits package including health, life, retirement, flexible time off, and much more!
Benefit from working in a highly collaborative and diverse environment, as well as within a welcoming and empowered team.
Clinical Trial Associate Jobs
By Glooko At ,
Ensure compliance with SOPs and regulatory requirements (e.g., GCP and US and OUS guidelines).
Participate in product improvement activities (information gathering, requirements, cross-functional meetings) that meet our customers' needs.
Bachelor's degree or equivalent in a related field with 1-2 years of experience in clinical trials.
Knowledge of digital health solutions and applications preferred.
Knowledge of the clinical research process preferred.
Excellent organization and customer service skills.
Clinical Trial Rater Jobs
By M3 USA At Los Alamitos, 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
Clinical Trial Manager/Sr. Clinical Trial Manager
By Akero Therapeutics At San Francisco Bay Area, United States
Relevant clinical trial experience in the pharmaceutical or health care industry or equivalent
Experience as the regional lead for Europe, United States, and/or India.
Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
This position is for remote work, but may require domestic or international travel as required (valid travel documents must be obtainable).
At least 4+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
Senior Research Analyst, Clinical Trial Entity Matching
By H1 At , Remote $55,000 - $65,000 a year
Detail-oriented and strong time-management skills
Bachelor’s Degree and 1-2 years of relevant experience in research, healthcare, data, or other related fields (Internship experience may be sufficient)
Knowledge of research methods, data analysis, quality metrics
Language skills is a plus
Biological, clinical, or medical experience is a plus
Drive change through informing R&C processes for profile creation from EM no match queues, starting with Clinical Trial data
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

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