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Clinical Trial Assistant Jobs

Clinical Trial Assistant/Sr. Clinical Trial Assistant
By Mineralys Therapeutics, Inc. At Greater Boston, United States
Assist with preparation of reports (management reports, regulatory reports, etc.), as required.
Quality Assurance, Data Management, Safety, Medical, Project Management
Provide support for day-to-day study activities in accordance with established protocols under the general guidance of the assigned Clinical Trial Manager
Help manage external vendors by setting up meetings, taking minutes, proactively communicating, and responding to requests.
Manage the oversight of sample collection and analysis (e.g., lab samples, PK samples)
Demonstrates working knowledge of clinical research conduct, laws, regulations, and standards, and complies with applicable SOP's and policies
Clinical Trial Assistant Jobs
By Abbott Laboratories At , San Diego, Ca $24 - $49 an hour
To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
Good organizational skills, ability to manage multiple tasks and meticulous attention to detail.
To provide general administrative support to the Clinical Affairs Department and assistance to department Manager(s) and Director(s).
Research or health care related academic or work experience preferable.
Good written and verbal communication skills.
To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals.
Clinical Trial Assistant Jobs
By Randstad Life Sciences US At Dallas-Fort Worth Metroplex, United States
Supports the clinical trial management/operational study teams in the execution and delivery of studies. Plan, direct, or coordinate clinical research projects.
Collect and track patient enrollment information and update study management reports as necessary
Generate reports in various applications to assist the Clinical Trial Managers to perform clinical data review
Experience as Clinical Trial Assistant/Associate
Strong skills with Microsoft Excel is required
Experience using electronic data capture (EDC) systems
Clinical Trial Coordinator Jobs
By DOCS At All, MO, United States
Document management, tracking, electronic filing and review
A relevant educational background, either in life-sciences or as a licensed healthcare professional
The ability to manage multiple priorities simultaneously
Have oncology trial experience will be a plus
Providing ongoing administrative support to other members of the clinical study team, supporting other clinical colleagues in tracking study progress
Collaborating with site staff to ensure clinical trials are being run according to the protocol
Clinical Trial Lead Jobs
By Avania At United States
Ability to work concurrently on multiple protocols and procedures; organizational, time management skills and problem-solving abilities
RN or BA/BS degree in a science/life science, engineering or health-related field plus a minimum 4 years monitoring experience
Experience as mentor and trainer for new CRAs
Excellent communication skills; demonstrated professional writing proficiency
Experience generating project-specific training presentations and coordinating necessary training
Ability to generate monitoring tools; experience generating and giving professional presentations
Research Assistant- Ptsd Phase Ii Clinical Drug Trial
By Boston Medical Center At , Remote
Exceptional written, verbal, telephone and interpersonal communication skills
Advertising and participant recruitment efforts
Telephone pre-screen participants for eligibility
Schedule participants for in-person visits
Administer psychological, psychophysiological, cognitive and memory assessments
Primary data collection and entry (qualitative and quantitative)
Clinical Trial Assistant Based In Warsaw - Hybrid
By DOCS At All, MO, United States
Document management, tracking, electronic filing and review
CTA experience or Project Associate or Coordinator experience in clinical trials on regional level in Europe
Administrative experience in clinical trials
Providing ongoing administrative support to other members of the clinical study team, supporting other clinical colleagues in tracking study progress
Collaborating with site staff to ensure clinical trials are being run according to the protocol
Ensuring studies are run according to ICH GCP and other applicable regulations at site
Clinical Trial Coordinator (Ctc)
By ICON At , Remote
Completed job training (office management, administration, finance, health care preferred) or B.A./B.S. (Life Science preferred) or equivalent healthcare experience
Highly effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request
Excellent negotiation skills for CTCs in finance area
Minimum 1-2 yrs in Clinical Research or relevant healthcare experience
Clinical Trial Nurse - Providence, Ri
By IQVIA At , Providence, Ri
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 Specialist Jobs
By Stryker At , , Mi $73,100 - $152,400 a year
Manage data, conduct routine site visits, ensure timely reporting of adverse events, generate, and distribute internal and external communication.
2+ years of clinical research experience as a Clinical Research Coordinator, Clinical Trial Coordinator, or Clinical Research Associate
Knowledge of FDA regulations and their practical implementation
Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
Self-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
Ensure reporting of adverse events from research site staff to the sponsor and the IRB/IEC

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