Medical Drug Information jobs
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- Bayshore HealthCareMississauga, ON
- $48,750–$65,000 a year
- Contract
- Provide and support medical information services and participates in coverage after business hours, as required.
- Support with audits as needed.
- Alberta Blue CrossEdmonton, AB
- Full-time
- Weekends as needed +1
- Interpret clinical information, accepted medical conditions, and plan criteria to ensure decisions are accurate, consistent, and clearly documented.
- Bayshore HealthCareMississauga, ON
- $48,750–$65,000 a year
- Provide and support medical information services and participates in coverage after business hours, as required.
- Apporter du soutien lors des audits, au besoin.
- View all Bayshore HealthCare jobs - Mississauga jobs - Coordonnateur Santé Et Sécurité (H/F) jobs in Mississauga, ON
- Salary Search: Coordinateur(trice) en SMIM - Drug Safety and Medical Information (DSMI) Coordinator salaries in Mississauga, ON
- See popular questions & answers about Bayshore HealthCare
View similar jobs with this employerAmazon Canada Fulfillment Services, ULCNisku, AB- $31.00–$51.77 an hour
- Assist with random saliva drug testing protocols.
- Provide first aid support and make referrals to outside medical providers as necessary.
- Alberta Blue CrossEdmonton, AB
- Full-time
- Overtime
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- Allergan AestheticsMontréal, QC
- Full-time
- Researching, analyzing and evaluating methods to disseminate medical and scientific information.
- Develops territory routing that effectively supports the…
- AbbVieToronto, ON
- $112,000–$162,000 a year
- Full-time
- Ensure a strong medical and scientific presence for AbbVie in investigational sites and key scientific centers by facilitation of clinical research and of…
- View all AbbVie jobs - Toronto jobs - Liaison jobs in Toronto, ON
- Salary Search: Pipeline Medical Science Liaison, Oncology salaries in Toronto, ON
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View similar jobs with this employerCencora, Inc.Ontario- Full-time
- Screening medical and scientific literature for safety information.
- Experience in the medical and/or pharmaceutical field(s), medical terminology is an asset;
- View all Cencora, Inc. jobs - Ontario jobs - Associate jobs in Ontario
- Salary Search: Drug Safety Associate salaries in Ontario
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- Abbott LaboratoriesMississauga, ON
- $75,750–$111,100 a year
- Full-time
- Experience with preparing and filing Class II-IV Canadian medical device license applications, Investigational Testing Applications and working knowledge of the…
- Cencora, Inc.Ontario
- Full-time
- Certification in medical information, drug information, pharmacovigilance, drug safety, or equivalent preferred.
- View all Cencora, Inc. jobs - Ontario jobs - Associate jobs in Ontario
- Salary Search: Pharmacovigilance Associate salaries in Ontario
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- サイネオス・ヘルスOntario
- Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer…
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- サイネオス・ヘルスOntario
- Conducts Source Document Review of appropriate site source documents and medical records.
- Collaborate with RWLP Regulatory team to ensure updated regulatory…
Professional Services Executive
Easily applySiemens HealthineersRemote- $99,500–$142,000 a year
- Full-time
- This information is provided per required laws and regulations.
- The Professional Services Executive (PSE) is an account success management role focused on…
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Pharmacovigilance Aggregate Report Manager
Easily applyApcer Life SciencesRemote- $60,000–$75,000 a year
- Trains and mentors’ new medical safety physician (if required).
- The position reports to the Delivery head of Otsuka aggregate project.
Pharmacovigilance Aggregate Report Manager
Easily applyApcer Life SciencesRemote- $60,000–$75,000 a year
- Trains and mentors’ new medical safety physician (if required).
- The position reports to the Delivery head of Otsuka aggregate project.
Indegene: Medical Information Manager (Canada)
Easily applyTrilogy Writing and ConsultingToronto, ON- $140,000–$160,000 a year
- Full-time
- Experience in managing others within medical information department.
- Knowledge of IRMS medical information database (preferred).
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Drug Safety and Medical Information (DSMI) Coordinator
Mississauga, ON
•
Remote
$48,750–$65,000 a year
-
Contract
Drug Safety and Medical Information (DSMI) Coordinator
Job details
$48,750–$65,000 a year
Contract
Remote in Mississauga, ON
Full job description
Drug Safety and Medical Information (DSMI) Coordinator(
Job Number:
26005980)Primary Location
:ON-Mississauga Pharma Employee Type:Contract Pay Rate From:$48,750 Pay Rate To:$65,000Description
:This is a contract opportunity with an anticipated end date of October 2027.
JOB SUMMARY
The Drug Safety and Medical Information (DSMI) Coordinator is responsible for managing AE/PV inbox and supporting the collection, processing, quality check and reporting of Safety events (Adverse Events and/or Product Quality Complaints) and handling Medical Information (MI) inquiries. The incumbent will represent the Scientific Affairs Department at Bayshore Specialty Rx both internally and externally as required and ensure compliance with Canadian Adverse Event reporting guidelines, Good Pharmacovigilance practices and Medical Information practices.
DUTIES AND RESPONSIBILITIES
The Drug Safety and Medical Information (DSMI) Coordinator is responsible for managing AE/PV inbox and supporting the collection, processing, quality check and reporting of Safety events (Adverse Events and/or Product Quality Complaints) and handling Medical Information (MI) inquiries. The incumbent will represent the Scientific Affairs Department at Bayshore Specialty Rx both internally and externally as required and ensure compliance with Canadian Adverse Event reporting guidelines, Good Pharmacovigilance practices and Medical Information practices.
DUTIES AND RESPONSIBILITIES
- Manage AE/PV inbox and conduct follow ups as required.
- Perform data entry of safety events into internal database (CRM).
- Retrieve source emails and source documents from the internal database.
- If needed, assist with collection, processing, quality check and reporting of Safety events (initial and follow-up) as per the program requirements.
- If needed, correct any errors that were identified in the submitted AE reports.
- If needed, conduct investigation for quality issues and collect all the information to complete CAPA.
- Conduct follow-ups for information from initial reporter and fill in gaps as necessary.
- If required, support with reconciliation activities as per the program requirements.
- If required, support/conduct activities related to source data verification as per the program requirements and/or PV agreement.
- Provide and support medical information services and participates in coverage after business hours, as required.
- Use available resources and FAQs to provide accurate and timely responses (verbal and/or written) to medical information queries.
- Ensure timely and compliant reporting of Adverse Events (AEs) and Product Quality Complaints (PQCs) in accordance with Health Canada pharmacovigilance requirements and guidelines, including accurate documentation, appropriate escalation, and effective collaboration with internal stakeholders and regulatory teams.
- Support with audits as needed.
- Build excellent rapport with the internal and external customers.
- Maintains confidentiality of patient, client, and corporate information at all times.
- Participates in proactive Health and Safety activities while performing all duties.
- Is responsible to notify immediate Supervisor of any Health and Safety risks or concerns.
- Employee will maintain relevant level of knowledge of ICH (International Conference on Harmonization), GDP (Good Documentation Practices), GCP (Good Clinical Practice), Health Canada GVP (Good Pharmacovigilance Practices), Health Canada Adverse Event Reporting guidelines, and familiarity with Canada Vigilance-MedEffect Program, as appropriate to their hired role which is to be provided at time of hire and on an as needed basis. With this knowledge the employee will perform the work as required by their assigned function and will be provided with regular updates as required.
- Participates in processes relating to regulatory and/or contractual reporting requirements.
- Adheres to Bayshore’s Policies and Procedures.
- Completes other tasks as requested/required.
Qualifications
:
QUALIFICATIONS
EDUCATION
Degree or Diploma in a health and life sciences related field or equivalent combination of education and healthcare experience.
EXPERIENCE
OTHER SKILLS AND ABILITIES
At Bayshore Healthcare, our commitment to Equity, Diversity & Inclusion is our strength. This is how we bring our vision of being the difference in the lives of those we care for, work with and in our communities. We have a great sense of pride in creating a culture of belonging, where individual differences are embraced and celebrated, through programs, resources and policies that support each individual's purpose, potential and wellbeing.
At Bayshore Healthcare Ltd., and its subsidiaries, we are committed to fostering an inclusive workplace and operate in full compliance with all Provincial and Territorial legislation pertaining to Human Rights Codes and Accessibility requirements. To ensure continued compliance throughout the recruitment and selection process, we encourage candidates to disclose any accommodation needs they may have.
EDUCATION
Degree or Diploma in a health and life sciences related field or equivalent combination of education and healthcare experience.
EXPERIENCE
- 1-2 years of PV experience or related Healthcare work experience (in Drug/Medical Information, Medical Affairs, Regulatory Affairs, Clinical Trials or Healthcare call center environment).
- Knowledge of Health Canada guidelines on Reporting Adverse Reactions for Marketed Health Products, Global PV regulations, ICH guidelines and Pharmacovigilance auditing.
OTHER SKILLS AND ABILITIES
- Excellent written, verbal communication and facilitation skills.
- Excellent organizational & critical thinking skills.
- Strong and proven attention to detail.
- Ability to work with strict timelines and handle multiple priorities.
- Flexible, adaptable, and able to work under pressure and convey a sense of urgency.
- Demonstrated initiative and accountability and be able to work under minimal supervision.
- Excellent customer service skills to deal with client questions, sometimes under difficult circumstances. Be able to handle challenging discussions.
- Team Player with ability to function in a multi-disciplinary environment and promote collaboration.
- Proficiency with basic computer skills, excel, PowerPoint, reporting tools etc. Prior experience with a Pharmacovigilance reporting software and/or safety databases applications an asset.
At Bayshore Healthcare, our commitment to Equity, Diversity & Inclusion is our strength. This is how we bring our vision of being the difference in the lives of those we care for, work with and in our communities. We have a great sense of pride in creating a culture of belonging, where individual differences are embraced and celebrated, through programs, resources and policies that support each individual's purpose, potential and wellbeing.
At Bayshore Healthcare Ltd., and its subsidiaries, we are committed to fostering an inclusive workplace and operate in full compliance with all Provincial and Territorial legislation pertaining to Human Rights Codes and Accessibility requirements. To ensure continued compliance throughout the recruitment and selection process, we encourage candidates to disclose any accommodation needs they may have.
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