Markham, On Master in biotechnology Jobs – 12 Openings This Week

Clinical Research Assistant
Everest Clinical Research —Markham, ON
- $45,000–$70,000 a year
- Microsoft Office
- Master's degree
- Bachelor's
- Disability insurance
- Dental care
Quick apply
Clinical Trial Assistant I
Everest Clinical Research —Markham, ON
- $45,000–$65,000 a year
- Remote
- Microsoft Office
- Administrative experience
- Bachelor's
- Disability insurance
- Dental care
Quick apply
Reproductive Research Assistant
Toronto Zoo —Toronto, ON
- $34.24–$38.04 an hour
- Weekends as needed
- Public speaking
- Laboratory experience
- Research
Quick apply
1d
Head of Data Governance - Product Line
Sanofi EU —Toronto, ON
- $165,800–$276,300 a year
- Azure
- Master's degree
- AWS
Clinical Data Management Specialist
Everest Clinical Research —Markham, ON
- $45,000–$70,000 a year
- Remote
- Master's degree
- Quality Control
- Data entry
- Disability insurance
- Dental care
Quick apply
Assistant Clinical Analyst I (Canada)
GeneDx —Toronto, ON
- $56.80–$62.93 an hour
- Remote
- Medicine
- Doctoral degree
- Computer literacy
Data Product Manager – Analytical Data Products
ShyftLabs —Toronto, ON
- $130,000–$160,000 a year
- Full-time
- Hybrid work
- Computer Science
- Engineering
- Master's degree
- Dental care
- Vision care
Quick apply
Computer Systems Validation
Pharmeng Technology Inc —Toronto, ON
- Windows
- Bachelor's
- Team management
Quick apply
Professor Firefighting
Seneca Polytechnic —North York, ON
- $77,153–$133,752 a year
- Immediate opening
- Engineering
- Research
- Master's degree
Senior Process Engineer
IPS-Integrated Project Services —Vaughan, ON
- Full-time
- AutoCAD
- Engineering
- Bachelor's
Head of Data Governance - Product Line
Sanofi —Toronto, ON
- $165,800–$276,300 a year
- Azure
- Master's degree
- AWS

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Clinical Research Assistant
Everest Clinical Research —Markham, ON
May assist with hardcopy and electronic archiving of clinical trial documents, including filing within a Trial Master File, according to established document…
$45,000–$70,000 a year
Quick apply
Clinical Trial Assistant I
Everest Clinical Research —Markham, ON
Interact with study Sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high-quality operationalization of clinical…
$45,000–$65,000 a year
Quick apply

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Clinical Research Assistant

Everest Clinical Research -
Markham, ON

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Job details

Permanent
$45,000–$70,000 a year

Qualifications

Record keeping
Clinical research
Filing
Microsoft Office
Master's degree
Bachelor's
Quality Control
File scanning and digitization
Project quality control reviews
Customer service orientation
Organizational skills
Data validation
Document management
Medical terminology
Communication skills

Full job description

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.

Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

To drive continued success in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning team as a Clinical Research Assistant for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

Key Accountabilities:

Receive medical writing and safety monitoring projects and project information from the Direct Manager or from the Work Mentor for the assigned projects. The project information may include the study protocol, Case Report Forms (CRFs), Investigator’s Brochure, etc.

Support medical writing and safety monitoring teams by performing QC review of document deliverables, including Clinical Study Reports (CSR), clinical study protocols, Informed Consent Forms, patient safety narratives, Safety Management Plans, scientific publications, and other documents intended for regulatory submissions.

Perform consistency review of document formats, styles, and overall layout according to a document style guide.

Perform data verification (QC) on statistical programming outputs against data source such as patient CRFs or other information provided. Report discrepancies found during the QC procedure.

Learn and perform document e-publishing for clinical trial and regulatory documents, including CSRs and tables, listings, and graphs (TLGs), which may include collection, scanning, electronic assembly, bookmarking, hyperlinking of documents, document cleaning, and header/pagination stamping, etc. Ensure the final product meets specific document publishing requirements and timelines.

May assist with hardcopy and electronic archiving of clinical trial documents, including filing within a Trial Master File, according to established document control and archiving practices.

May act as a DMC/DSMB Secretary, producing meeting minutes and assisting the DMC/DSMB Administrator to plan, organize, and coordinate meetings and serve as the primary contact for day‑to‑day operations between the members and the Sponsor.

Plan and manage deliverables and timelines in accordance with clinical trial project teams’ requirements.

Keep current on the training of Everest Guidance Documents and with the general requirements or guidelines issued by the pharmaceutical drug trial regulators and ICH.

Qualifications and Experience:

Bachelor degree in Clinical or Medical or Life Sciences with experience in the subject matter. M.Sc. or higher preferred.

Clinical trial experience in a pharmaceutical or Clinical Research Organization environment preferred.

Experience in Phase I through Phase IV clinical trials with knowledge of drug/medical device regulations and industry standards.

Experience with an accepted clinical data capture and management system preferred.

Strong verbal and written communication skills with the ability to understand and summarize medical terminology.

Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.

Ability to maintain a high degree of confidentiality with clinical data and client’s proprietary data.

Detail-oriented, customer- and quality-focused.

Excellent interpersonal and teamwork skills.

Computing skills in Microsoft Office applications preferred.

Proven flexibility and adaptability when working in a team and independently, using good judgment in making decisions, preferred.

Benefits & Compensation:

We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.

Estimated Salary Range: $45,000 - $70,000.

To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com (http://www.everestclinical.com)

We thank all interested applicants, however, only those selected for an interview will be contacted.

Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.

#LI-Remote
#LI-KD1

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master in biotechnology jobs in markham, on

Clinical Research Assistant

Clinical Trial Assistant I

Reproductive Research Assistant

Head of Data Governance - Product Line

Clinical Data Management Specialist

Assistant Clinical Analyst I (Canada)

Data Product Manager – Analytical Data Products

Computer Systems Validation

Professor Firefighting

Senior Process Engineer

Head of Data Governance - Product Line

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