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Clinical Trials Assistant Jobs in Ontario

Clinical Trials Manager Jobs
By Spectral Medical Inc. At Etobicoke, Ontario, Canada
4 plus years of experience in clinical trial management
Knowledge of the clinical trial process. Knowledge of ICH guidelines and GCP including basic understanding of regulatory requirements
Oversight and management of day-to-day trial operations including CRO management
Oversight and management of certain sub-studies that may be undertaken from time to time
Management of trials and oversight of day-to-day trial operations (70%)
Management of Study Team Members (15%)
Protocol Writer - Clinical Trials
By Pharma Medica Research Inc. At Mississauga, Ontario, Canada
Must possess good computer skills and organizational skills. Experience with an electronic document control and management system would be a plus.
Ensure timely and accurate entries and updates into a computer management system required for clinical conduct.
3 or more years of pharmaceutical related experience in medical writing, preferably in a CRO.
Thorough knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines.
Strong knowledge of medical terminology, clinical trials, and clinical research.
Strong knowledge of processes with a desire to promote improvement. Ability to motivate and energize others with a positive, can-do attitude.
Medical Advisor Clinical Trials 002
By Alexion Pharmaceuticals, Inc. At Mississauga, Ontario, Canada
Minimum 5 years of combined experience in Medical Affairs/Clinical Operations/Clinical Development
Knowledge of the country’s healthcare system and market access environment
Plan and manage complex projects
Knowledge of clinical trial conduct
Previous experience in rare diseases is of advantage
Ensuring appropriate and compliant level of Patient Advocacy Organization (PAO) group involvement with Patient Advocacy team
Clinical Administrative Assistant Jobs
By Get Gambit At London, Ontario, Canada
Post-secondary education (Bachelor’s degree or Technical diploma) preferred; certification in medical administration is a plus.
Excellent communication and interpersonal skills with an ability to work effectively in a remote, digital environment.
Proven experience as an administrative assistant, preferably in a virtual healthcare environment.
Strong customer service skills and empathy for patients, particularly in understanding the unique healthcare needs of men.
Exceptional organizational skills and attention to detail.
Support virtual clinical operations by managing administrative tasks, including patient scheduling, data entry, and digital record-keeping.
Clinical Trials Quality Specialist
By Hamilton Health Sciences At Hamilton, Ontario, Canada
Systematic thinker with strong project management and organizational skills
Experience with modifying, implementing, validating, and maintaining a web-based Clinical Trials Management System, including trouble shooting operational problems
Experience with, or certification in Lean or Six Sigma considered an asset
Recognized certification in clinical research (ACRP or SOCRA) preferred
Minimum five (5) years clinical research experience in a health care setting
Minimum three (3) years cancer related experience

Are you looking for an exciting opportunity to join a dynamic team and help advance medical research? We are looking for a Clinical Trials Assistant to join our team and help us make a difference in the lives of patients. As a Clinical Trials Assistant, you will be responsible for providing administrative and operational support to clinical trials and research studies. You will have the chance to work with a variety of stakeholders, including physicians, nurses, and other healthcare professionals. If you are passionate about making a difference in the lives of patients and have a strong attention to detail, this could be the perfect job for you!

A Clinical Trials Assistant is a professional who works in the clinical research field, assisting with the planning, coordination, and execution of clinical trials. They are responsible for ensuring that the trials are conducted in accordance with the protocol and applicable regulations. They may also be responsible for data collection, data entry, and other administrative tasks. To become a Clinical Trials Assistant, you should have a bachelor’s degree in a related field, such as healthcare administration or clinical research. You should also have experience in clinical research and be familiar with the regulations and guidelines that govern clinical trials. Skills required for a Clinical Trials Assistant include strong organizational and communication skills, attention to detail, and the ability to work independently. Knowledge of clinical research protocols and regulations is also important. Responsibilities of a Clinical Trials Assistant include coordinating and scheduling clinical trials, collecting and entering data, and ensuring that the trials are conducted in accordance with the protocol and applicable regulations. Experience in clinical research is beneficial, as is knowledge of medical terminology and clinical trial software. Qualifications for a Clinical Trials Assistant include a bachelor’s degree in a related field, such as healthcare administration or clinical research. You should also have experience in clinical research and be familiar with the regulations and guidelines that govern clinical trials. Tools that help Clinical Trials Assistants work more effectively include clinical trial software, such as eClinicalWorks, which helps to streamline the process of collecting and entering data. Other tools include project management software, such as Asana, which helps to keep track of tasks and deadlines. Good tips to help Clinical Trials Assistants do their job more effectively include staying organized, staying up to date on the latest regulations and guidelines, and communicating clearly with the research team. Common Clinical Trials Assistant interview questions include: What experience do you have in clinical research? What do you know about the regulations and guidelines that govern clinical trials? What do you think makes you a good fit for this position?