Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...
Senior Clinical Trial Manager
Markham, ON · On-site
... Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer * At least 3 years ...
Quick apply
Senior Clinical Trial Manager
Markham, ON · On-site
... Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer * At least 3 years ...
... Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer * At least 3 years ...
... Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer * At least 3 years ...
Job Overview CRA's Life Sciences practice helps pharmaceutical, biotechnology, diagnostics, and ... Conduct primary and secondary research to identify, collect, manage and analyze data to identify ...
Job Overview CRA's Life Sciences practice helps pharmaceutical, biotechnology, diagnostics, and ... Conduct primary and secondary research to identify, collect, manage and analyze data to identify ...
Clinical Associate - Hybrid Role - French Speaking - Toronto, Canada ICON is a global healthcare ... research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
Clinical Associate - Hybrid Role - French Speaking - Toronto, Canada ICON is a global healthcare ... research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
... research & development services to global pharmaceutical and biotech companies, developing their ... The QA Associate - Biologics is accountable to the QA Manager, Biologics and plays a key role in ...
Quick apply
... research & development services to global pharmaceutical and biotech companies, developing their ... The QA Associate - Biologics is accountable to the QA Manager, Biologics and plays a key role in ...
... research & development services to global pharmaceutical and biotech companies, developing their ... The QA Associate - Biologics is accountable to the QA Manager, Biologics and plays a key role in ...
... research & development services to global pharmaceutical and biotech companies, developing their ... The QA Associate - Biologics is accountable to the QA Manager, Biologics and plays a key role in ...
Associate Talent Sourcing Specialist 6-Month Contract Location: Leeds, UK or Warsaw, Poland Help ... research organizations (CROs), we help pharmaceutical, biotechnology, and medical device companies ...
Associate Talent Sourcing Specialist 6-Month Contract Location: Leeds, UK or Warsaw, Poland Help ... research organizations (CROs), we help pharmaceutical, biotechnology, and medical device companies ...
Conduct primary research interviews and extract insights for team discussion strategic ... pharmaceutical or biotech arena (Industry or life sciences consulting). Progressively more ...
Conduct primary research interviews and extract insights for team discussion strategic ... pharmaceutical or biotech arena (Industry or life sciences consulting). Progressively more ...
Manage external research vendors and consultants to deliver results * Lead localization and de novo ... biotechnology, vaccines or healthcare industry * As part of Moderna's commitment to build a ...
Manage external research vendors and consultants to deliver results * Lead localization and de novo ... biotechnology, vaccines or healthcare industry * As part of Moderna's commitment to build a ...
Lead the team for Market Research to ensure primary data helps direct efforts appropriately and ... biotechnology company with demonstrated mastery of analytical responsibilities is required.
Lead the team for Market Research to ensure primary data helps direct efforts appropriately and ... biotechnology company with demonstrated mastery of analytical responsibilities is required.
Summary Reporting to the Associate Director, Marketing- Rare Disease, the Product Manager will help ... Design, and execute marketing research needs to generate insights that can drive the strategic plan
Summary Reporting to the Associate Director, Marketing- Rare Disease, the Product Manager will help ... Design, and execute marketing research needs to generate insights that can drive the strategic plan
Senior Equipment Technician
CA$22.40 - CA$30.80/hr
Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent ... Prior experience with biotechnology equipment is strongly preferred Knowledge, Skills, and ...
Senior Equipment Technician
CA$22.40 - CA$30.80/hr
Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent ... Prior experience with biotechnology equipment is strongly preferred Knowledge, Skills, and ...
Sr. Product Manager, Canada
Toronto, ON · On-site
... research, sales force assessments, targeting assessments, positioning, messaging and OPEX budget ... Work with General Manager and Associate Marketing Director to help set sales forecasts and provide ...
Sr. Product Manager, Canada
Toronto, ON · On-site
... research, sales force assessments, targeting assessments, positioning, messaging and OPEX budget ... Work with General Manager and Associate Marketing Director to help set sales forecasts and provide ...
... companies in the clinical R&D phase to large public biopharma's. Common accounting areas ... Understand skillsets and capabilities of Senior Associates and Supervisors andmonitorand review ...
... companies in the clinical R&D phase to large public biopharma's. Common accounting areas ... Understand skillsets and capabilities of Senior Associates and Supervisors andmonitorand review ...
Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active ...
Quick apply
Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active ...
Research Associate Biotech information
See Ontario salary details
$11.30 - $15.14
3% of jobs
$15.14 - $18.99
6% of jobs
$22.21 is the 25th percentile. Wages below this are outliers.
$18.99 - $22.84
18% of jobs
$22.84 - $26.68
16% of jobs
The median wage is $28.31 / hr.
$26.68 - $30.53
14% of jobs
$33.72 is the 75th percentile. Wages above this are outliers.
$30.53 - $34.38
20% of jobs
$34.38 - $38.22
11% of jobs
$38.22 - $42.07
4% of jobs
$42.07 - $45.91
3% of jobs
$45.91 - $49.76
2% of jobs
$49.76 - $53.61
1% of jobs
$11
$30
$53
How much do research associate biotech jobs pay per hour?
What is a research associate biotech?
A Research Associate in Biotechnology is responsible for conducting experiments, analyzing data, and supporting scientific research in areas such as pharmaceuticals, genetics, and molecular biology. They work in laboratories, using advanced equipment and techniques to develop new products, improve existing processes, or contribute to scientific discoveries. Typical tasks include preparing samples, running assays, documenting results, and collaborating with scientists and engineers. This role requires a strong background in biology, chemistry, or a related field, along with attention to detail and problem-solving skills.
What are the typical daily responsibilities of a research associate biotech?
As a Research Associate in Biotech, your daily responsibilities often include conducting laboratory experiments, preparing and analyzing samples, recording and interpreting data, and maintaining detailed lab notebooks. You may also be responsible for ensuring the smooth operation of laboratory equipment and adhering to strict safety and quality protocols. Collaboration is common, so you’ll regularly interact with scientists, lab managers, and other team members to discuss findings or help design new experiments. This role offers variety and the chance to actively contribute to innovative research projects that could advance new biotechnological solutions.
What are the key skills and qualifications needed to thrive in the research associate biotech position?
To thrive as a Research Associate in Biotech, you need a solid background in molecular biology, biochemistry, or a related field—typically supported by a bachelor's or master’s degree. Experience with laboratory techniques such as PCR, cell culture, and analytical instrumentation, as well as familiarity with data analysis software and laboratory information management systems, is often required. Strong attention to detail, problem-solving abilities, and effective teamwork and communication skills set candidates apart. These competencies are crucial for ensuring high-quality research results, maintaining lab safety, and driving successful collaboration within scientific teams.
What are popular job titles related to Research Associate Biotech jobs in Ontario?
For Research Associate Biotech jobs in Ontario, the most frequently searched job titles are:
What job categories do people searching Research Associate Biotech jobs in Ontario look for?
The top searched job categories for Research Associate Biotech jobs in Ontario are:
What cities in Ontario are hiring for Research Associate Biotech jobs?
Cities in Ontario with the most Research Associate Biotech job openings:

Full-time
Medical, Retirement, PTO
Re-posted 21 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
13th of 74 rated research
Job description
Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Montreal Canada. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work.
This is a home-based position in Montreal Canada.
Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.
WE OFFER THE FOLLOWING
- Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives
- Voluntary retirement scheme
- Home office furniture allowance, mobile phone and hotspot for internet access anywhere
- In-house travel agents, reimbursement for airline club and TSA pre-check
- Customized PACE training program based on your experience and therapeutic background and interest
- User friendly CTMS with electronic submission and approval of monitoring visit reports
- Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
- National assignments with average of 2 protocols
- In-house administrative support for all levels of CRAs
- Opportunities to work with international team of CRAs
- Low turnover rates for CRAs
- No metric for minimum required days on site per month
- Flexible work hours across days within a week
- Opportunity for CRA leadership positions - Lead CRA, CRA Manager
- Many additional perks unmatched by other CROs!
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
- Maintain ongoing site correspondence and site files;
- Complete visit reports and maintaining study-related databases;
- Oversight and interaction with clinical research sites; and
- Review of patient charts and clinical research data.
- Bachelor's degree in science from an accredited university;
- At least 2 years as a Clinical Research Associate or Clinical Research Coordinator;
- Bilingual in English and French;
- Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations;
- Excellent interpersonal, written and verbal communication skills in English and French;
- Strong attention to detail and organization skills;
- Highly motivated, independent, flexible;
- Ability to travel between 60-80%;
- Ability to prioritize workload to meet timelines across multiple studies; and
- Proficient in Microsoft Office.
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
-
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
-
- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992