Clinical Study Start Up Specialist - (Permanent Full Time)
By Ontario Institute for Cancer Research At Greater Toronto Area, Canada
At least 1 year of experience in data coordination of oncology clinical trials
Excellent prioritization skills, excellent computer skills, ability to learn quickly and work independently
Knowledge of applicable legislative, UHN and/or departmental policies
Certification as a Clinical Research Professional, preferred.
At minimum, a completion of a Bachelor’s degree program, or recognized equivalent in Health or Science Related Discipline
Ability to work under pressure and perform multiple concurrent tasks with a high level of attention to detail
Greentech Founder At Your Own Start-Up (100 % Remote) (M/F/D)
By EWOR At Vancouver, British Columbia, Canada
We have partnered with renowned companies like Lufthansa that will assist you in your (future) responsibilities by offering industry-specific support.
You will go through an intense personal development and coaching journey with our education team and mentors.
This is a remote opportunity, no relocation required.
You will found, build, and run your own start-up in fields such as GreenTech.
We require a commitment of at least 20 hours per week from you to ensure your venture's success.
We take you on a 10-month learning journey that is designed for highly motivated individuals who aspire to become successful founders.
Study Delivery Associate (Hybrid - Mississauga)
By ICON Strategic Solutions At Greater Toronto Area, Canada
You are part of the vendor selection and management process where appropriate
You prepare and execute Statement of Work (SOW) with vendor for local drug management
University degree in Health Science, or a related field (an equivalent combination of education, training, and work experience may be considered)
You review, discuss, and communicate packaging and labelling requirements, as defined by the protocol, with vendors
Two years experience in Clinical Research or related industry
Strong social and interpersonal skills (written and oral). You will be confident speaking to Health Care Professionals.
Warehouse Associate - Earn Up To $20.75/Hr
By ClickJobs.io At Deep Cove, British Columbia, Canada
Earn more: You can expect a competitive wage and reliable paycheck when you work for Amazon.
Stay active: You’ll be on the move for your whole shift in our fast-paced environments.
High school, GED, or equivalent diploma
Warehouse Associate - Earn Up To $20.75/Hr
By ClickJobs.io At Brentwood Bay, British Columbia, Canada
Earn more: You can expect a competitive wage and reliable paycheck when you work for Amazon.
Stay active: You’ll be on the move for your whole shift in our fast-paced environments.
High school, GED, or equivalent diploma
Warehouse Associate - Earn Up To $20.75/Hr
By ClickJobs.io At Victoria, British Columbia, Canada
Earn more: You can expect a competitive wage and reliable paycheck when you work for Amazon.
Stay active: You’ll be on the move for your whole shift in our fast-paced environments.
High school, GED, or equivalent diploma
Warehouse Associate - Earn Up To $20.75/Hr
By ClickJobs.io At View Royal, British Columbia, Canada
Earn more: You can expect a competitive wage and reliable paycheck when you work for Amazon.
Stay active: You’ll be on the move for your whole shift in our fast-paced environments.
High school, GED, or equivalent diploma
Warehouse Associate - Earn Up To $20.75/Hr
By ClickJobs.io At Saanichton, British Columbia, Canada
Earn more: You can expect a competitive wage and reliable paycheck when you work for Amazon.
Stay active: You’ll be on the move for your whole shift in our fast-paced environments.
High school, GED, or equivalent diploma
Start-Up Lead 2 (Gta - Remote)
By ICON Strategic Solutions At Greater Toronto Area, Canada
Prepare and submit regulatory and IRB/IEC documentation as required per country requirements and Bayer QSDs during the course of the study
Strong written and verbal English communication skills
Demonstrated organization skills and attention to detail
Ability to work independently and manage multiple tasks and priorities
**This is a remote-based position but candidates MUST reside in the Greater Toronto Area
Benefits of Working in ICON:

Are you looking for an exciting opportunity to jumpstart your career in the research industry? We are looking for a Study Start Up Associate I to join our team and help us launch clinical trials with speed and accuracy. You will be responsible for ensuring that all study start up activities are completed in accordance with applicable regulations and guidelines. If you have a passion for research and a drive to make a difference, this is the perfect job for you!

Overview:

Study Start Up Associate I is responsible for the coordination and management of clinical trial start up activities. This includes working with internal and external stakeholders to ensure that all study start up activities are completed in a timely and compliant manner.

Detailed Job Description:

Study Start Up Associate I is responsible for the coordination and management of clinical trial start up activities. This includes working with internal and external stakeholders to ensure that all study start up activities are completed in a timely and compliant manner. The Study Start Up Associate I will be responsible for the following tasks:

• Developing and maintaining study start up timelines
• Coordinating and managing the collection of essential documents
• Ensuring that all study start up activities are completed in a timely and compliant manner
• Liaising with internal and external stakeholders to ensure that all study start up activities are completed in a timely and compliant manner
• Ensuring that all study start up activities are completed in accordance with applicable regulations and guidelines
• Assisting with the preparation of study start up documents
• Assisting with the preparation of study start up budgets
• Assisting with the preparation of study start up contracts
• Assisting with the preparation of study start up reports
• Assisting with the preparation of study start up presentations
• Assisting with the preparation of study start up materials
• Assisting with the preparation of study start up training materials
• Assisting with the preparation of study start up communications
• Assisting with the preparation of study start up meetings
• Assisting with the preparation of study start up audits

What is Study Start Up Associate I Job Skills Required?

• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Ability to work under pressure and meet deadlines
• Knowledge of clinical trial regulations and guidelines
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial software and systems
• Knowledge of clinical trial budgeting and contracting
• Knowledge of clinical trial reporting and presentations
• Knowledge of clinical trial materials and training
• Knowledge of clinical trial communications
• Knowledge of clinical trial meetings and audits

What is Study Start Up Associate I Job Qualifications?

• Bachelor’s degree in a related field
• At least 2 years of experience in clinical trial start up activities
• Knowledge of applicable regulations and guidelines
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial software and systems
• Knowledge of clinical trial budgeting