Study Start Up Lead
Mississauga, ON · On-site
As a key member of our Country Study Start-Up team, you will drive and facilitate the efficient initiation of clinical trials, ultimately helping to deliver innovative treatments to patients. The ...
Mississauga, ON · On-site
As a key member of our Country Study Start-Up team, you will drive and facilitate the efficient initiation of clinical trials, ultimately helping to deliver innovative treatments to patients. The ...
Mississauga, ON · On-site
As a key member of our Country Study Start-Up team, you will drive and facilitate the efficient initiation of clinical trials, ultimately helping to deliver innovative treatments to patients. The ...
Study start-up experience with Health Canada and Ethics submissions; * Knowledge of ICH guidelines and applicable local regulations; and * Proficiency in English and French is a plus. Medpace ...
Study start-up experience with Health Canada and Ethics submissions; * Knowledge of ICH guidelines and applicable local regulations; and * Proficiency in English and French is a plus. Medpace ...
Hamilton, ON · On-site
Study Start Up * Create/revise/test/approve Case Report Forms (CRFs), and Reference pages ... Conduct conference calls with the Sponsor and Clinical Research Associates for site updates.
Hamilton, ON · On-site
Study Start Up * Create/revise/test/approve Case Report Forms (CRFs), and Reference pages ... Conduct conference calls with the Sponsor and Clinical Research Associates for site updates.
Ensures and/or affirms study start up documentation aligns with Data Standards and Standard Operating Procedures (SOPs) * Develops and/or ensures quality in the database design including both CRF and ...
Ensures and/or affirms study start up documentation aligns with Data Standards and Standard Operating Procedures (SOPs) * Develops and/or ensures quality in the database design including both CRF and ...
Request, collect, and organize essential clinical research documents from study start-up to closure. * Facilitate the publication review process and support ongoing project timelines and budgets.
Request, collect, and organize essential clinical research documents from study start-up to closure. * Facilitate the publication review process and support ongoing project timelines and budgets.
Toronto, ON · On-site
CA$125K - CA$150K/yr
... start-up processes, Tarion warranty administration, performance audits, reserve fund study procurement, and governance support. The role is instrumental in driving operational excellence, continuous ...
Toronto, ON · On-site
CA$125K - CA$150K/yr
... start-up processes, Tarion warranty administration, performance audits, reserve fund study procurement, and governance support. The role is instrumental in driving operational excellence, continuous ...
Carry out or oversee thermodynamic studies, including mass and energy balances, efficiency ... Develop, update, and validate operating, start-up and shutdown, and lockout and tagout procedures ...
Carry out or oversee thermodynamic studies, including mass and energy balances, efficiency ... Develop, update, and validate operating, start-up and shutdown, and lockout and tagout procedures ...
Carry out or oversee thermodynamic studies, including mass and energy balances, efficiency ... Develop, update, and validate operating, start-up and shutdown, and lockout and tagout procedures ...
Carry out or oversee thermodynamic studies, including mass and energy balances, efficiency ... Develop, update, and validate operating, start-up and shutdown, and lockout and tagout procedures ...
CA$90K - CA$105K/yr
They will also develop process metrics to evaluate and improve plant performance, provide start-up ... Studies methods in current use to do process calculations and makes improvements and/or develops ...
CA$90K - CA$105K/yr
They will also develop process metrics to evaluate and improve plant performance, provide start-up ... Studies methods in current use to do process calculations and makes improvements and/or develops ...
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
CA$850/wk
Many studies offer compensation, which varies by study type and duration Compensation: * Up to $850 ... start, we invite you to submit your interest online today. Important Notice - No Fees Required:
$8.65 - $14.66
18% of jobs
$17.05 is the 25th percentile. Wages below this are outliers.
$14.66 - $20.67
18% of jobs
$20.67 - $26.68
14% of jobs
The median wage is $27.02 / hr.
$26.68 - $32.69
9% of jobs
$32.69 - $38.70
7% of jobs
$38.70 - $44.71
4% of jobs
$44.71 - $50.72
3% of jobs
$51.97 is the 75th percentile. Wages above this are outliers.
$50.72 - $56.73
6% of jobs
$56.73 - $62.74
2% of jobs
$62.74 - $68.75
5% of jobs
$68.75 - $74.76
13% of jobs
$8
$37
$74
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
For Study Start Up Associate jobs in Ontario, the most frequently searched job titles are:
The top searched job categories for Study Start Up Associate jobs in Ontario are:

9.3
Based on 23 frontline employees who took The Breakroom Quiz
3rd of 86 rated pharmaceutical
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The PositionAt Roche Pharma Product Development Global Clinical Operations (PDG), we are determined to transform drug development and realize our Pharma Ambition to deliver 20 transformative medicines addressing diseases with the highest societal burden by 2029. Every role here connects to something real: the health and lives of patients.
As a key member of our Country Study Start-Up team, you will drive and facilitate the efficient initiation of clinical trials, ultimately helping to deliver innovative treatments to patients.
The Opportunity:
You will lead the country strategy in a disease area for study start-up, driving efficiency, innovation, and collaboration with external stakeholders.
You will oversee start-up operations to ensure timely and efficient site activation and regulatory compliance.
You will identify and lead opportunities for process automation, standardization, and innovation at both the country and site levels.
You will collaborate with regional and global counterparts to harmonize systems and improve timelines.
You will oversee the development and management of clinical trial submissions and amendments, ensuring regulatory coordination.
You will provide strategic oversight for all aspects of budgeting and contract management, including developing budget strategies and negotiating with internal and external stakeholders.
You will participate in external industry collaborations to influence the country's start-up environment.
Who You Are:
You have a degree (MD, PhD, MA/MS, BA/BS) in life sciences or a related field with 1-3 years of experience in submissions, and cross-functional collaboration.
You have demonstrated experience in clinical trial start-up
Proven track record in managing site relationships with a customer centric mindset andmanaging complex clinical trials start-up
You possess a strong understanding of ICH-GCP, EU CTR, and local regulatory environments.
You have excellent communication, interpersonal, and problem-solving skills, with a collaborative mindset.
Fluency in written and spoken English is mandatory
Ability to manage multiple priorities and work in a fast-paced, dynamic environment.
Ability to travel if needed.
Preferred:
A postgraduate degree in clinical trials or clinical research is highly desirable.
Relocation Benefits are not available for this job posting.
The expected salary range for this position based on the primary location of Mississauga is 89,256.00 and 117,148.50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.We use artificial intelligence to screen, assess or select applicants for this role.
This posting is for an existing vacancy at Hoffmann-La Roche Ltd.
Who we areA healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
Roche is an Equal Opportunity Employer.