Remote Biotechnology Jobs – 94 Openings This Week

Senior Biostatistician
Everest Clinical Research —Markham, ON
- $110,000–$160,000 a year
- Remote
- Doctoral degree
- Master's degree
- Project management
- Disability insurance
- Dental care
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Principal Biostatistician
Everest Clinical Research —Markham, ON
- $150,000–$200,000 a year
- Doctoral degree
- Master's degree
- Continuous improvement
- Disability insurance
- Dental care
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Biology Specialist
Turing —Remote
- $100–$200 an hour
- Contract
- Remote
- Doctoral degree
- No experience needed
- Bachelor's
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3d
Medical Writer
BGBx —Remote
- $75,000–$105,000 a year
- Full-time
- Remote
- Medicine
- Doctoral degree
- Research
- Paid time off
- Life insurance
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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
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Associate Quality Engineer
Veeva Systems —Remote
- $55,000–$95,000 a year
- Full-time
- Remote
- Java
- SQL
- No university degree
- Designated paid holidays
- Dental care
5d
Clinical Trial IWRS Monitor I
Everest Clinical Research —Markham, ON
- $45,000–$65,000 a year
- Databases
- Quality Control
- In-person
- Disability insurance
- Dental care
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Assistant Clinical Analyst I (Canada)
GeneDx —Toronto, ON
- $56.80–$62.93 an hour
- Remote
- Medicine
- Doctoral degree
- Computer literacy
Clinical Coordinator
Tiny Health —Toronto, ON
- Full-time
- Remote
- Bachelor's
- Organizational skills
- Pediatrics
Quick apply
13d
Bioinformatics Analyst
DNAstack —Toronto, ON
- $100,000–$150,000 a year
- Full-time
- Remote
- Azure
- Engineering
- Research
- Dental care
- Vision care
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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
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Medical Writer
Everest Clinical Research —Markham, ON
- $65,000–$100,000 a year
- Remote
- Microsoft Word
- Doctoral degree
- Master's degree
- Disability insurance
- Dental care
Quick apply
Bioinformatics Technician
Tiny Health —Toronto, ON
- Part-time
- Remote
- Master's degree
- SQL
- AWS
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Medical Science Liaison, Dermatology, British Columbia
AbbVie —Vancouver, BC
- $110,000–$160,000 a year
- Full-time
- Remote
- Medicine
- Microsoft Outlook
- Doctoral degree
Clinical Trial Manager, Clinical Operations, Infectious Disease
Moderna, Inc. —Toronto, ON
- Full-time
- Databases
- Bachelor's
- Organizational skills
- Designated paid holidays
- Paid time off
2d
Research Scientist, Health Economic Modeling
Precision Medicine Group —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Doctoral degree
Physician Operations Coordinator
Centricity Research —Remote
- $55,000–$60,000 a year
- Full-time
- Remote
- English
- Business development
- Travel
Quick apply
8d
Medical Science Liaison, Dermatology (Southwest Ontario & Manitoba) - 12 Month Contract
AbbVie —Toronto, ON
- $103,000–$181,500 a year
- Full-time
- Remote
- Medicine
- Microsoft Outlook
- Doctoral degree
Senior Medical Writer
BGBx —Toronto, ON
- $100,000–$125,000 a year
- Full-time
- Remote
- Research
- Travel
- Communication skills
- Paid time off
- Life insurance
Quick apply
1d
Senior Manager, Global Quality Assurance
Medexus Pharma —Remote
- $140,000–$180,000 a year
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Master's degree

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Senior Biostatistician

Everest Clinical Research -
Markham, ON

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Job details

Permanent
$110,000–$160,000 a year

Qualifications

Data quality auditing
Statistics
Clinical research
Doctoral degree
Data quality assurance
Master's degree
Statistical analysis
Project management
Report and presentation preparation
Quality Control
Project quality control reviews
Data validation rules
Performing statistical data analysis
Standard operating procedures (SOPs)

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 committed, skilled, and customer-focused individuals to join our winning team as Senior Biostatisticians for our Markham, Ontario on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

Key Accountabilities:

1. Leadership and Project Management:

Lead efforts in resolving day to day work related issues and problems, securing quality, improving efficiency and productivity of statistical and programming operations.

Lead assigned projects by applying project management skills, statistical and programming techniques; achieve quality and on time delivery of deliverables, earn client’s trust and repeat business.

2. Statistical Planning and Methodologies:

Provide statistical expertise for design, analysis and reporting of clinical trials and research projects.

Contribute to the writing of statistical sections of study protocols, perform sample size calculation, develop randomization specifications, and generate randomization codes.

Write Statistical Analysis Plans (SAPs) and properly address Peer Statistician review comments.

Create and maintain Statistical and Programming Quality Control (QC) and QA Plans for assigned projects.

Provide input to unblinded data management plan when required.

Assist in research and development of statistical methodologies and processes.

3. Statistical Programming:

Develop and/or review ADaM dataset specifications. Review and provide input to SDTM dataset specifications when required.

Perform QC validation of analysis datasets and TLGs.

Perform third level review of dry runs and final run.

Lead statistical dry runs and final run by actively participating or contributing to project and resources management, addressing statistical and programming questions and interacting with data management to follow up and resolve data issues.

Review and provide input to the Analysis Data Reviewer’s Guide, discuss and incorporate Data Standards Reviewer’s review comments to ensure quality of the document.

4. Statistical Analysis and Reporting, and Publication Support:

Perform statistical analysis as per SAP, and address peer/QC review comments and findings.

Perform statistical validation of core results, address additional QC validation comments and findings on the core results.

Plan and conduct or contribute to the trial results reporting/dissemination meetings.

Under supervision contribute to the contents describing any deviation from the planned analysis and deviation from study conduct for the Clinical Study Report (CSR). Review CSR to ensure accuracy, completeness and appropriateness of the interpretation of the statistical results.

Write statistical report or statistical sections of the CSR.

Perform statistical analyses for publications, including but not limited to abstracts, manuscripts, presentations and posters.

5. Supporting Clinical Data Collection and Cleaning:

Provide statistical input to Case Report Forms (CRF) design and database/variable structure.

Provide statistical input to non-CRF data collection and acquisition methods and approaches.

Review Data Management Plan sections relating to critical data collection and cleaning. Provide statistical input to Data Validation Specification.

Specify and/or program database quality acceptance checks, assess and report data quality issues, and follow through until resolution.

Perform ongoing assessment and communication of data quality issues, including protocol deviations.

Assist data management and trial management team in preparing for database lock.

6. Complete job required and project-specific training. Comply with applicable Everest and trial sponsor’s policies, SOPs, and work instructions.

7. Properly archive study files in accordance with trial sponsor’s requirements.

8. Plan and carry out professional development activities.

Qualifications and Experience:

A Ph.D. degree in statistical science, mathematical analysis or related fields plus 2 years highly relevant experience or a Master’s degree plus 4 years highly relevant experience, with demonstrated ability and sustained performance.

Everest is inviting candidates to apply to this existing vacancy.

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: $110,000 - $160,000.

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

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Refine Your Search

biotechnology jobs in remote

Senior Biostatistician

Principal Biostatistician

Biology Specialist

Medical Writer

Clinical Trial Assistant I

Associate Quality Engineer

Clinical Trial IWRS Monitor I

Assistant Clinical Analyst I (Canada)

Clinical Coordinator

Bioinformatics Analyst

Clinical Data Management Specialist

Medical Writer

Bioinformatics Technician

Medical Science Liaison, Dermatology, British Columbia

Clinical Trial Manager, Clinical Operations, Infectious Disease

Research Scientist, Health Economic Modeling

Physician Operations Coordinator

Medical Science Liaison, Dermatology (Southwest Ontario & Manitoba) - 12 Month Contract

Senior Medical Writer

Senior Manager, Global Quality Assurance

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