
501 - 1000 employees
💼 Consulting
🏥 Healthcare
💊 Pharmaceuticals
💰 Private equity on 2021-05
Consulting • Healthcare • Pharmaceuticals
Veristat is a clinical development services company that provides end-to-end, regulatory-focused support for biopharmaceutical and medical device sponsors. The firm offers full-service clinical trial planning and conduct, regulatory affairs and submission support (including NDA/MAA and interactions with agencies like PMDA), statistical and biometrics services, medical writing, pharmacovigilance, and project management for complex therapeutic areas such as oncology, rare diseases, neurology, biologics, and cell & gene therapies. Veristat operates as a B2B partner to biotech and pharmaceutical organizations to reduce development risk and accelerate regulatory approval.
🕒 October 5
🇨🇦 Canada – Remote
💵 $92k - $107k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
👻 Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

501 - 1000 employees
💼 Consulting
🏥 Healthcare
💊 Pharmaceuticals
💰 Private equity on 2021-05
Consulting • Healthcare • Pharmaceuticals
Veristat is a clinical development services company that provides end-to-end, regulatory-focused support for biopharmaceutical and medical device sponsors. The firm offers full-service clinical trial planning and conduct, regulatory affairs and submission support (including NDA/MAA and interactions with agencies like PMDA), statistical and biometrics services, medical writing, pharmacovigilance, and project management for complex therapeutic areas such as oncology, rare diseases, neurology, biologics, and cell & gene therapies. Veristat operates as a B2B partner to biotech and pharmaceutical organizations to reduce development risk and accelerate regulatory approval.
• Perform analysis of clinical trial data • Provide statistical input into reporting of clinical trial results • Work largely independently with minimal oversight from the Director or Manager of Biostatistics, or Senior Biostatistician • Apply statistical methods to Phase I-IV clinical trials • Manage multiple tasks under tight timelines
• PhD degree in Statistics, Biostatistics, or related field with relevant academic experience OR a Master’s degree in Statistics or Biostatistics or a related field and 3 years of biostatistical experience in the clinical trials or health research environment OR a Bachelor’s degree in Statistics, Biostatistics or a related field and 5 years of biostatistical experience in a clinical research organization in a hands-on technical position with a demonstrated ability to perform the duties above • Excellent written and oral communication skills including grammatical/technical writing skills • Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials • SAS proficiency including BASE and STAT; GRAPH preferred • Proficiency in Microsoft Word and Excel • Strong level of detail orientation • Ability to work on multiple tasks under tight timelines
• Remote working • Flexible time off • Paid holidays • Medical insurance • Tuition reimbursement • Retirement plans • Applicable bonus
Apply Now🕒 October 2
Clinical Research Associate monitoring Canadian clinical trials for Parexel, a global clinical research organization. Managing site relationships, compliance, data quality, and study delivery.
🗣️🇫🇷 French Required
🕒 October 2
Clinical Research Associate monitoring sponsor-dedicated clinical trials at ICON, the global clinical research organization. Ensuring protocol compliance, data integrity, and patient safety across trial sites.
🕒 October 1
Senior Clinical Scientist authoring clinical and regulatory documents for Indero, a global dermatology and rheumatology CRO. Supporting study design, data interpretation, submissions, and scientific teams.
🕒 October 1
Clinical Trial Manager overseeing Parexel clinical trials, vendors, sites, documentation, and regulatory compliance. Supporting trial execution from initiation through closeout in Ontario.
🕒 September 29
Senior Clinical Research Associate monitoring investigator sites and ensuring GCP-compliant clinical trial execution. Supporting patient safety, recruitment, data quality, and study close-out for Parexel.