MetaPharm Clinical Research

Careers

Careers at MetaPharm

Join a collaborative CRO team that values scientific passion, quality, and long-term partnership with sponsors and sites.

Clinical teams

Clinical teams

Cross-functional culture

Cross-functional culture

Culture

  • Quality-driven clinical research environment
  • Cross-functional learning across operations, data, and regulatory
  • Opportunity to work on diverse therapeutic programs
  • Collaborative culture with low turnover and project continuity

Benefits

  • Competitive compensation
  • Professional development and training
  • Flexible hybrid work options where applicable
  • Exposure to global studies coordinated from Canada

Open roles

26+ opportunities across clinical operations, data, regulatory, and quality.

Apply now

Clinical Research Associate

Canada (Hybrid/Field) · Full-time

Monitor clinical trial sites, ensure ICH-GCP compliance, and support high-quality data collection across assigned studies.

Apply

Senior Clinical Research Associate

Canada (Field) · Full-time

Lead complex site monitoring visits, mentor junior CRAs, and drive inspection-ready documentation standards.

Apply

Clinical Trial Assistant

Canada / Hybrid · Full-time

Support TMF maintenance, site correspondence, visit logistics, and day-to-day study operations.

Apply

Clinical Project Manager

Canada · Full-time

Own end-to-end study delivery with cross-functional teams, sponsors, and investigator sites.

Apply

Senior Clinical Project Manager

Canada · Full-time

Lead multi-study portfolios, manage budgets and timelines, and serve as primary sponsor contact.

Apply

Clinical Operations Manager

Canada · Full-time

Oversee CRA resources, monitoring strategy, and operational KPIs across active programs.

Apply

Feasibility Manager

Remote / Canada · Full-time

Run country and site feasibility, enrollment modeling, and investigator outreach for new studies.

Apply

Study Start-Up Specialist

Canada · Full-time

Coordinate ethics submissions, contracts, site activation packages, and green-light readiness.

Apply

Patient Recruitment Specialist

Canada / Hybrid · Full-time

Design and execute site-level recruitment tactics to meet enrollment goals on schedule.

Apply

Clinical Data Manager

Remote / Canada · Full-time

Lead EDC build and data cleaning activities, preferably with Medidata Rave experience, through database lock.

Apply

EDC Programmer (Medidata Rave)

Remote / Canada · Full-time

Build eCRFs, edit checks, and custom functions; support UAT and mid-study changes.

Apply

Lead Clinical Data Manager

Canada · Full-time

Own data management plans, vendor oversight, and database lock strategy for complex trials.

Apply

Biostatistician

Canada · Full-time

Support study design, sample size, SAP development, and interpretation of clinical results.

Apply

SAS® Statistical Programmer

Remote / Canada · Full-time

Develop validated ADaM/SDTM datasets, TFLs, and reproducible analysis programs.

Apply

CDISC Standards Specialist

Remote / Canada · Contract

Guide SDTM/ADaM mapping, define.xml, and submission-ready dataset packages.

Apply

Medical Writer

Remote / Canada · Full-time

Author protocols, informed consent, CSRs, and regulatory documents to ICH standards.

Apply

Senior Medical Writer

Canada · Full-time

Lead complex writing programs, peer review deliverables, and mentor junior writers.

Apply

Pharmacovigilance / Safety Associate

Canada · Full-time

Process SAEs, support reconciliation, and maintain safety reporting timelines.

Apply

Medical Monitor

Canada / Hybrid · Full-time

Provide medical oversight, protocol guidance, and safety signal review for assigned trials.

Apply

Quality Assurance Specialist

Canada · Full-time

Support SOP lifecycle, internal audits, CAPA tracking, and inspection readiness.

Apply

Clinical Quality Auditor

Canada (Travel) · Full-time

Conduct GCP audits of sites, vendors, and internal processes with clear CAPA follow-up.

Apply

Training & Compliance Coordinator

Canada / Hybrid · Full-time

Manage GCP training curricula, competency tracking, and compliance documentation.

Apply

Regulatory Affairs Specialist

Canada · Full-time

Support CTA/IND strategies, Health Canada and FDA interactions, and submission packages.

Apply

Regulatory Submissions Manager

Canada · Full-time

Plan and publish electronic submissions, maintain eCTD structure, and track agency queries.

Apply

Business Development Manager

Canada / Remote · Full-time

Identify sponsor opportunities, craft proposals, and grow long-term CRO partnerships.

Apply

Contracts & Proposal Specialist

Canada · Full-time

Prepare budgets, RFPs, and MSA/CSA language aligned to study scope and risk.

Apply
Join the MetaPharm team

Apply now

Tell us about your background and the role you are interested in. Attach your resume if available — our team will review your application and respond shortly.