We are currently looking for a Medical Advisor/Medical Affairs Lead for one of our prominent pharmaceutical clients based out of Thornhill, Ontario
Contract duration: 12-15 months Location: Thornhill, ON/Toronto/GTA - Hybrid or Quebec (Remote)
Role: The Medical Advisor (or Medical Affairs Lead) in Injectables Aesthetic (IA) plays a pivotal role in ensuring the successful medical, scientific, and strategic execution of IA portfolio including in line product and future assets. This position bridges science, clinical practice, and strategy, ensuring that all medical affairs activities are grounded in robust evidence, regulatory compliance, and aligned with our client's mission to advance dermatology for every skin story.
Key Responsibilities: Scientific and Clinical Leadership Serves as the medical and scientific expert for portfolio of injectable aesthetic products (e.g., neuromodulators, hyaluronic acid fillers, and biostimulators injectables). Provides evidence-based guidance on clinical data, product differentiation, and emerging science to internal teams (Marketing, Sales, Regulatory) and external stakeholders (HCPs, KOLs, professional societies). Translates complex data into actionable insights that support safe clinical practice and optimal patient outcomes. Medical Strategy and Cross-Functional Partnership Leads creation and execution of the medical affairs plan that underpins brand plans, ensuring scientific integrity and alignment with global aesthetic vision and strategic imperatives. Collaborates closely with commercial, training, and regulatory teams to ensure evidence-based positioning and compliant educational activities. Provides comprehensive trainings on products and related diseases to internal staff ensuring accurate delivery for study interpretation and objection handling Education and Scientific Engagement Designs and oversees medical education programs, speaker trainings, and scientific workshops that elevate injector expertise and patient safety standards across Canada. Engages with Key Opinion Leaders (KOLs) and clinical experts to build partnerships, gather insights, and co-create scientific content that advances the field. Supports development and dissemination of scientific narratives, publications, and presentations at national and regional congresses. Compliance and Governance Ensures all medical and promotional activities adhere to Canadian regulations and internal governance frameworks. Acts as a medical signatory and reviewer for materials requiring scientific validation and approval. Evidence Generation and Insights Identifies data gaps and contributes to clinical research initiatives, including investigator-initiated studies, real-world evidence projects, and post-marketing studies. Collects and interprets field medical insights to inform strategy, innovation, and lifecycle management of aesthetic products.
Skills & Qualifications: Medical, Pharmacy, Nurse Practitioner or higher degree qualification (e.g. MSc, PhD) in a relevant life sciences field Dermatology and Aesthetics experience is essential Proven several years (ideally minimum 5-10 years) related medical and/or research and development experience in the pharmaceutical, biotechnology, medical devices industry Demonstrable experience of developing and presenting scientific/medical content at a variety of levels, including to practicing clinical peers and seniors Good communication and presentation skills Meeting planning and facilitation skills and Ability to interface effectively with a variety of technical platforms Bilingual in English and French is an asset Ability to develop good relationships and credibility with medical professionals 20% travel requirement
We are currently looking for a Medical Advisor/Medical Affairs Lead for one of our prominent pharmaceutical clients based out of Thornhill, Ontario
Contract duration: 12-15 months Location: Thornhill, ON/Toronto/GTA - Hybrid or Quebec (Remote)
Role: The Medical Advisor (or Medical Affairs Lead) in Injectables Aesthetic (IA) plays a pivotal role in ensuring the successful medical, scientific, and strategic execution of IA portfolio including in line product and future assets. This position bridges science, clinical practice, and strategy, ensuring that all medical affairs activities are grounded in robust evidence, regulatory compliance, and aligned with our client's mission to advance dermatology for every skin story.
Key Responsibilities: Scientific and Clinical Leadership Serves as the medical and scientific expert for portfolio of injectable aesthetic products (e.g., neuromodulators, hyaluronic acid fillers, and biostimulators injectables). Provides evidence-based guidance on clinical data, product differentiation, and emerging science to internal teams (Marketing, Sales, Regulatory) and external stakeholders (HCPs, KOLs, professional societies). Translates complex data into actionable insights that support safe clinical practice and optimal patient outcomes. Medical Strategy and Cross-Functional Partnership Leads creation and execution of the medical affairs plan that underpins brand plans, ensuring scientific integrity and alignment with global aesthetic vision and strategic imperatives. Collaborates closely with commercial, training, and regulatory teams to ensure evidence-based positioning and compliant educational activities. Provides comprehensive trainings on products and related diseases to internal staff ensuring accurate delivery for study interpretation and objection handling Education and Scientific Engagement Designs and oversees medical education programs, speaker trainings, and scientific workshops that elevate injector expertise and patient safety standards across Canada. Engages with Key Opinion Leaders (KOLs) and clinical experts to build partnerships, gather insights, and co-create scientific content that advances the field. Supports development and dissemination of scientific narratives, publications, and presentations at national and regional congresses. Compliance and Governance Ensures all medical and promotional activities adhere to Canadian regulations and internal governance frameworks. Acts as a medical signatory and reviewer for materials requiring scientific validation and approval. Evidence Generation and Insights Identifies data gaps and contributes to clinical research initiatives, including investigator-initiated studies, real-world evidence projects, and post-marketing studies. Collects and interprets field medical insights to inform strategy, innovation, and lifecycle management of aesthetic products.
Skills & Qualifications: Medical, Pharmacy, Nurse Practitioner or higher degree qualification (e.g. MSc, PhD) in a relevant life sciences field Dermatology and Aesthetics experience is essential Proven several years (ideally minimum 5-10 years) related medical and/or research and development experience in the pharmaceutical, biotechnology, medical devices industry Demonstrable experience of developing and presenting scientific/medical content at a variety of levels, including to practicing clinical peers and seniors Good communication and presentation skills Meeting planning and facilitation skills and Ability to interface effectively with a variety of technical platforms Bilingual in English and French is an asset Ability to develop good relationships and credibility with medical professionals 20% travel requirement
Overview We are currently recruiting for our client based out of Edmonton for a contract role in planning / scheduling : Duration : 12 months T4 contract Location : Edmonton, AB Role : Participates in establishing initial construction plan by implementing templates and facilitating interactive planning sessions with key construction team members. Prepares drafts of network logic diagrams for segments or the construction phase as applicable. Performs forward and backward pass assessments during the preparation of the construction phase schedule and provides critical path analysis highlighting pertinent start and finish dates of milestones and activities. Compiles, organizes construction planning information and prepares the related construction schedule versions with different levels of detail and criteria including the weekly, bi-weekly look ahead and general construction schedule. Applies standard techniques, procedures, and criteria in carrying out EVM tasks supporting in a timely and accurate manner the project controls and construction management efforts. Utilizes Primavera P6 as scheduling and reporting tool. Assists with the resource loading process of the applicable construction scopes. Reviews short-cycle schedule impacts and prepares CPM project schedule analysis. Collects, validates, and integrates schedule and earned value progress information from vendors and contractors. Conducts progress audits by routine project walkthroughs. Prepares different tabular and graphical construction schedule timeline and resources reports as required. Assists in developing alternatives to accommodate changes and priorities. Attends construction meetings and participates by providing the applicable reports. Facilitates meetings with key construction project team members, vendors, and contractors to address and update the construction schedule status and forecast. Assists the home office staff with the coordination, monitoring, reporting and oversight of the field activities. Requirements Bachelor's degree in engineering, construction management, or a related field. Senior Engineer / Manager with 10+ years of experience working as Planning / Scheduling Engineer in EPC projects in the oil and gas, petrochemicals, industrial gases industries. Strong leadership skills and experience in leading teams at construction site, monitor and reporting schedules, managing subcontractors, stakeholder management. Proficiency in Primavera P6 scheduling software. Proven experience in the application of project management principles and techniques, including schedule development, resource management and earned value management. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Ability to work effectively in a team environment. #J-18808-Ljbffr
