Posted 10 hours ago
Remote Study Start-Up Project Manager - Canada
@ Medpace, Inc.
Canada
Overview
Medpace is hiring a full-time Study Start-Up Project Manager in Canada to run global start-up activities for clinical trials. The role covers regulatory submissions, Health Canada and ethics filings, and informed consent forms. The posting mentions an office-based culture with occasional work from home after training, and benefits that vary by country.
Responsibilities:
- Manage all aspects of global study start-up
- Perform quality checks on submission and site essential documents
- Prepare and approve informed consent forms
- Serve as sponsor point of contact for start-up and regulatory items
- Present at bid defenses, capabilities meetings and audits
Requirements summary:
- Bachelor's degree in a science or health-related field
- At least 5 years of CRO study start-up lead or manager experience
- Health Canada and ethics submission experience
- Knowledge of ICH guidelines and local regulations
- English and French proficiency is a plus
Tools & skills
Benefits mentioned
Source and dates
Source type not verified · jibe
- Employer posting date
- 2026-11-09
- First seen by our source
- 2026-11-09
- Source record updated
- 2026-11-09
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Project management |
| Experience | 5+ years |
| Hours per week | 40 (estimated) |
| Travel | air: minimal · ground: none |
| Work setting | Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English, French |
| Education | Bachelor’s degree (required) |
| Fields of study | science, health-related field |
| Perks mentioned | Generous paid time off, Retirement plan, Visa sponsorship, Wellness, Paid training |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Medpace, Inc.
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Accelerating Drug, Biologic and Medical Device Clinical Development
Full company description
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,200 people across 46 countries.
- LinkedIn followers
- 348,484
- People associated on LinkedIn
- 6,347
- Reported office locations
- 5375 Medpace Way, Cincinnati, OH 45227, US
- Business categories
- Clinical Trials
- Biotechnology
- Pharmaceutical
- Other recorded names
- Medpace, Inc.
- Medpace
- Specialties
- Early Phase Clinical Research
- Phase II-III Clinical Research
- RWE-Late Phase Clinical Research
- Medical Device and Diagnostics
- Regulatory Affairs
- Medical Writing
- Clinical Monitoring
- Clinical Trial Management
- Biostatistics and Data Sciences
- Drug Safety and Pharmacovigilance
- Quality Assurance
- Central Laboratories
- Bioanalytical Laboratories
- Imaging & ECG Core Labs
- Oncology clinical development
- Nephrology clinical development
- Neuroscience clinical development
- Infectious Disease clinical development
- Cardiovascular clinical development
- Metabolic and endocrine clinical development
- Rare disease clinical development
- Cell and gene therapy clinical development
- and Radiopharmaceuticals
- Profile identifies a recruitment agency
- No
- Reported total investment
- 0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and…
| Field | Value |
|---|---|
| Industry | Pharmaceutical Manufacturing |
| Company size | 5,001-10,000 employees |
| Headquarters | Cincinnati, OH |
| Organization type | Public Company |
| Year founded | 1992 |
| Specialties | Early Phase Clinical ResearchPhase II-III Clinical ResearchRWE-Late Phase Clinical ResearchMedical Device and DiagnosticsRegulatory AffairsMedical WritingClinical MonitoringClinical Trial ManagementBiostatistics and Data SciencesDrug Safety and Pharmacovigilance |
| Open jobs on Jobsy | 4 |
| View page |
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Clinical Operations team in Canada. This position plays a key role in the clinical trial management process at Medpace. With our continued growth in Canada, we are looking for proactive, positive, and self-motivated individuals with a shared commitment to quality to join our supportive and dynamic team.
Responsibilities
- Efficiently manage and successfully execute all aspects of global start-up;
- Perform quality checks on submission documents and site essential documents;
- Prepare and approve informed consent forms;
- Serve as a Sponsor point of contact for start-up and regulatory submissions items;
- Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
- Present during bid defenses, general capabilities meetings, and audits
Qualifications
- Bachelor’s degree in a science or health-related field;
- At least 5 years of study start-up Lead/Manager experience at a CRO;
- Study start-up experience with Health Canada and Ethics submissions;
- Knowledge of ICH guidelines and applicable local regulations; and
- Proficiency in English and French is a plus.
Medpace Overview
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
- 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
- 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.
- Efficiently manage and successfully execute all aspects of global start-up;
- Perform quality checks on submission documents and site essential documents;
- Prepare and approve informed consent forms;
- Serve as a Sponsor point of contact for start-up and regulatory submissions items;
- Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
- Present during bid defenses, general capabilities meetings, and audits
- Bachelor’s degree in a science or health-related field;
- At least 5 years of study start-up Lead/Manager experience at a CRO;
- Study start-up experience with Health Canada and Ethics submissions;
- Knowledge of ICH guidelines and applicable local regulations; and
- Proficiency in English and French is a plus.
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