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Biotechnology Research Associate Jobs in Alberta

Biotechnology Research Associate information

What does a Biotechnology Research Associate do?

A Biotechnology Research Associate supports scientific research projects in the field of biotechnology. Their responsibilities typically include conducting experiments, analyzing data, maintaining laboratory equipment, and preparing reports or presentations about research findings. They often work under the supervision of senior scientists and collaborate with other research staff. This role is essential in both academic and industry settings, as it helps drive innovation in areas such as medicine, agriculture, and environmental science.

What opportunities for professional growth and advancement are available to Biotechnology Research Associates?

Biotechnology Research Associates often have opportunities to advance by taking on more complex research projects, specializing in niche areas such as genomics or cell culture, or pursuing supervisory roles. Many organizations encourage continued education and may support attendance at conferences or workshops to stay current with emerging technologies. Collaborating closely with senior scientists and cross-functional teams also helps expand skill sets and build valuable professional networks, opening pathways to roles such as Research Scientist or Project Manager.

What is the difference between Biotechnology Research Associate vs Laboratory Technician?

AspectBiotechnology Research AssociateLaboratory Technician
Required CredentialsBachelor’s or Master’s in Biology, Biotechnology, or related fieldAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, academic institutionsClinical, industrial, or research laboratories
Employer & Industry UsageUsed in biotech research, pharmaceutical development, academiaCommon in clinical labs, manufacturing, quality control

The Biotechnology Research Associate typically holds a higher degree and engages in experimental design and data analysis, whereas Laboratory Technicians focus on routine testing and sample preparation. Both roles are essential in biotech and lab settings, but the Research Associate often takes on more complex research tasks.

What are the key skills and qualifications needed to thrive as a Biotechnology Research Associate, and why are they important?

To thrive as a Biotechnology Research Associate, you need a solid background in molecular biology, biochemistry, or related fields, usually supported by a bachelor's or master's degree. Familiarity with laboratory equipment, data analysis software, and techniques such as PCR, gel electrophoresis, and cell culture is typically required. Strong attention to detail, critical thinking, and effective teamwork are essential soft skills in this role. These skills and qualities are crucial for producing reliable research results, ensuring safety and compliance, and contributing meaningfully to scientific advancements.
What are popular job titles related to Biotechnology Research Associate jobs in Alberta? For Biotechnology Research Associate jobs in Alberta, the most frequently searched job titles are:
What job categories do people searching Biotechnology Research Associate jobs in Alberta look for? The top searched job categories for Biotechnology Research Associate jobs in Alberta are:
Infographic showing various Biotechnology Research Associate job openings in Alberta as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Bilingual Clinical Research Associate (CRA)

Medpace, Inc.

Calgary, AB • Hybrid

Other

Medical, Retirement, PTO

Posted 23 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 72 rated research


Job description

Job Summary

Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Alberta or British Columbia 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 Alberta or British Columbia 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!
Responsibilities
  • 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.  
Qualifications
  • Bachelor's degree in science from an accredited university;
  • At least 1 year 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 Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

  • Flexible work environment 
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Awards

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Medpace logo

About 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