Drug Safety Associate

Innomar Strategies Inc.; Canada; Remote; CAD 55,000 - 75,000; Full time

Job summary

Innomar Strategies Inc. is seeking a Drug Safety Associate for remote Canada. You will support patient and provider safety data, review adverse event information, and ensure compliant data handling across CANADA markets.

The role requires 1–3 years in medical information, clinical research or drug safety, strong analytical and communication skills, and a detail-oriented, deadline-driven mindset. Bilingual English/French is a plus.

Qualifications

• Minimum college level education; a Life Sciences concentration is a strong asset.
• 1–3 years in Medical Information, Clinical Research or Drug Safety.
• Knowledge of pharmacovigilance guidelines (Health Canada, US FDA, EMEA, ICH).
• Bilingual English/French is an asset.
• Experience in medical/pharmaceutical fields is an asset.

Responsibilities

• Receive, scan and document clinical information in compliance with SOPs.
• Work directly with internal and external clients to request information or clarification as necessary.
• Review source data documents and triage adverse events and product quality complaints.
• Data entry and submission of adverse event information into program databases.
• Sorting and filing of incoming documents; perform quality checks as directed.
• Assist with source data verification checks.
• Screen medical/scientific literature for safety information.
• Prepare reconciliation reports and conduct follow-up letters and clarifications.
• Assist and participate in non-conformance/CAPA processes.
• Transcription, translations and redaction activities.

Skills

Strong analytical skills

Effective communication

Interpersonal skills

Organizational skills

Attention to detail

Deadline-oriented

Problem-solving

MS Office proficiency

Education

College diploma in Life Sciences

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Office suite

Job description

## Drug Safety AssociateApply: Remote, ON: Full time: Posted Today: R2617957Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!# **Job Details**This role is in support of Cencora’s patient and provider support and pharma commercialization services in Canada marketed through our Innomar Strategies business.# **Responsibilities:*** Receive, scan and document all pertinent clinical information in compliance with SOP/protocol and applicable legislation* Work directly with internal and external clients to request additional information or clarification as necessary;* Review of source data documents (includes visit report/PIR review) and triaging adverse event information and product quality complaints as per client needs;* Data entry and submission of adverse event information and product quality complaints into program specific databases;* Sorting and filing of incoming documents;* Perform quality check on adverse event reports as directed by the work instructions.* Assist with and/or perform source data verification checks* Screening medical and scientific literature for safety information* Preparation of Reconciliation (weekly, monthly etc.) Reports* Transcription, translations and redaction activities* Preparation and conducting solicited follow-up letters and data clarifications* Assist and participate in the non-conformance/CAPA process* The Drug Safety Associate will also be assigned other duties and tasks as required from time to time.**Education*** Minimum college level education required. A diploma or degree with a concentration in Life Sciences is a strong asset; **Work Experience:*** 1-3 years experience in Medical Information, Clinical Research or Drug Safety or equivalent and related experience in pharmacy or pharmaceutical fields;* Knowledge of Pharmacovigilance industry including up to date knowledge of; pharmacovigilance guidelines of Health Canada, US FDA, EMEA and ICH;* Adaptability to change and to learn new skills as required;* Experience in the medical and/or pharmaceutical field(s), medical terminology is an asset;* Bilingual, English/French is an asset. **Skills & Knowledge*** Strong analytical skills* Ability to communicate effectively both orally and in writing.* Effective interpersonal skills.* Effective organizational skills; ability to multitask.* Superior, proven attention to detail.* Ability to consistently meet deadlines.* Excellent problem-solving skills; ability to communicate and/or resolve issues effectively and efficiently* Computer skills (including knowledge of Microsoft Word, Excel, PowerPoint and other Office Programs)* Good internet required for remote work.# **What Cencora offers**We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.