Job SummaryThis role is a temporary 18 - Month contract.The Study Coordinator has the overall responsibility for the technical conduct of a study, as well as for the documentation and reporting of results. The Study Coordinator represents the single point of study control.The Study Coordinator will demonstrate an ability to not only perform duties requiring a high level of technical skill, but also show complete understanding of research, the objectives of the research being conducted, and be able to independently organize the equipment, staff, space and their own time to ensure that all deliverables are met. This position will be able to independently review study procedures and be able to conduct them without supervision. This position will also be able to train and lead other staff in study procedures.The Study Coordinator will also be able to identify possible flaws in study design, and report those flaws to the Scientific Director or Study Director. Supervisory duties may apply to this role at the discretion of the Rodent Department Manager. The SC Supervisor will collaborate with the Rodent Department Manager on the supervision and training of assigned Research Technicians, and oversee scheduling of personnel within the Rodent Department on study procedures. The SC Supervisor will have the capabilities of performing, assisting and training on most assigned rodent facility and technical tasks.Duties And ResponsibilitiesKey ActivitiesStudy CoordinatorOversee, organize, implement and conduct various aspects of research studies.Coordinate and monitor study activities to ensure success and timely completion.Develop the skills to plan, design, and conduct studies.Coordinate sample analysis with internal and external laboratories, shipping and/or couriers while ensuring study timelines are maintained.Review study results and coordinate statistical analysis and reporting of results with Scientific Directors and/or technical report writers.Well versed in Microsoft Office suite (Excel, Word, Powerpoint)Develop and prepare study documentation to support carrying out of in-vivo studies such as study protocols, AUMs, etc.Formulate test articles with knowledge of basic chemistry principles, proficient with dosage calculations, mathematical manipulation and communicate results back to sponsors, as required.Work with internal Quality Control and contractor's QAU to ensure that studies are adequately monitored.Data entry, quality control and basic data analysis.Develop and revise relevant SOPs as requested.Perform technical procedural work as required at the Research Technician II level (basic and advanced).Train staff on various procedures as appropriate.Able to lead and/or support new model development to meet sponsor needsMaintain sufficient inventory and ordering of suppliesParticipate in internal working groups (animal care committee, health & safety, CTLS etc.).Inform Rodent Department Manager of department or operational issues or concerns and assist them in the maintenance and operation of animal facility and husbandry in accordance with CCAC guidelines, Animals for Research Act and facility SOPsSupport internal and external recruitment process based on TPC standards and policies as appropriateAssume functions of various personnel as dictated by staffing requirements for individual studies and trainingScheduling appropriately trained personnel for tasksAbility to explain and/or demonstrate processes and techniques to new employees and visitors.Other duties as assignedSupervisorCarry out performance management (PMR) of assigned research techniciansLead matters pertaining to human resources including performance reviews (PMR), corrective actions, accident reports,



etcEnsure research technician training is scheduled, completed and kept up to dateRecognize when re-training is due and plan for productive scheduling of re-training with little to no interruption to department objectivesSupport and collaborate scheduling of research technicians for operational and study tasks, together with Rodent Department Manager and Study Coordinators, in order to carry out most efficient completion of daily expectationsDuties associated with the Rodent WingGeneral techniques:Operate centrifuges and perform advanced blood separation.Drug administration (SC, IM, IP, IV, PO, IN, IT, intradermal, etc.)Survival blood collection (saphenous, tail snip, submandibular, catheter, etc.)Terminal blood collection, CSF sampling, tissue/organ extraction and weighingAnaesthesia/AnalgesiaEuthanasiaRestrain animals for procedures as neededSurgery Skills (an asset): Perform aseptic surgical procedures from start to end independently, including but not limited to:Incisional SurgeryAmygdala Electrode ImplantationParathyroid Lesion SurgeryWound Healing SurgeryMass Removal SurgeryGastrointestinal Surgical Models (ie. GI catheterization, Bile Duct/Gallbladder catheterization, etc)Vascular catheterization (ie. Jugular, Carotid, Femoral, Portal, etc)CNS Surgical models (ie. ICV, EEG, Intrathecal dose administration, serial CSF collection via catheterization, etc)Epilepsy/Seizure Testing: Perform seizure testing from start to end independently, including but not limited to:6HzMESSC PTZCorneal KindlingAmygdala KindlingOperant Testing (where applicable):Lead operant testing and training in rodentsLead operant testing and training with staffDiagnose and repair box mechanical issuesOperant data interpretation/presentationBehavioural Testing:Prepare rooms and supplies for testingPossess proficiency to operate test apparatus for behavioural and cognitive testing (LMA, rotarod, grip strength, core body temperature, watermaze, EPT, PPI, Moseq, as well as software application as it relates to the test, etc.)Various behavioural assessments and scoringEEG Systems: DSI and TaiNiConduct daily observations (health observations)), if requiredRodent Abuse Liability (as applicable):General Behavioural AssessmentsPlace ConditioningIV and Oral Self-administrationDependence and withdrawal assessmentAdvanced formulation skillsSurgery support, recovery, and endpoint monitoringProficient in JVC catheter implantation surgeryAssembly, maintenance, validation, and implantation of surgical devicesWorking with controlled substancesData Management:Ability to create basic graphs from experimental results using ExcelUnderstand basic data analysis (means, standard error, median, interquartile)Any other duties as deemed necessaryINTERACTIONThis position requires coordination of resources (i.E. staff, equipment, space) with other Research Technicians, Animal Care Technicians, Study Coordinators, Scientific Directors and Rodent Department Manager. It also requires the ability to learn new skills and procedures as well as teach skills efficiently.COMMUNICATIONCommunications are with the Scientific Director, Study Sponsor, Rodent Department Manager and other facility staff and employees within the organization. Collaboration, execution, and reporting of the quality assurance program.



Verbal communication is required to request and receive instructions for work, to report on activities, results, problems, and to participate in planning and scheduling of work and equipment use. Written communication is required for accurate and detailed recording of procedures, for reporting results and for completing documentation. Preparation, reading, and comprehension of written protocols and manuals is essential.Responsibility For The Work Of OthersThe Study Coordinator/Supervisor will be responsible for the work of subordinates, to ensure industrially acceptable levels of performance and report concerns regarding non-subordinate staff to the Rodent Department Manager and/or Human Resources.RESPONSIBILITY FOR THE CARE OF INDIVIDUALSThe Study Coordinator/Supervisor will be responsible for enforcing company policies aimed to ensure the safety and well-being of TPC employees.WORKING CONDITIONSThere will be occasional periods of several hours per day exposed to noxious odours from diagnostic/anesthetic materials and/or samples. There will also be the occasional need to work with chemicals in a controlled environment under chemical fume hoods and/or biosafety cabinet. There will be the occasional exposure to small quantities of toxic irritant or corrosive chemicals as well as exposure to freezers (-80°C) while storing and retrieving materials.Physical RequirementsPHYSICAL DEMANDSLifting animals in and out of cages on a regular basis, carrying liquid containers, carrying boxes weighing up to 20 kg and daily periods of keyboarding.PHYSICAL DEXTERITYAgility, accuracy, and consistency will be required while handling precision instruments such as, pipettes, balances, pH meters, surgical instruments. Strong fine motor skills in fingers, hands, and arms.QualificationsEDUCATIONVeterinary diploma or B.Sc. degree in a relevant field (e.G., Pharmacology, Pharmacokinetics, Veterinary Sciences, Biochemistry) or relevant direct experience.CALAS- RLAT Certified and/or Member in Good Standing (strongly encouraged)EXPerienceProven organizational skills and attention to detailDemonstrated ability to communicate effectively orally and in writingDemonstrated ability to work in a team environment and to meet timelinesExperience as a Research Technician II for at least 1 year or relevant experienceExperience within a laboratory environmentExperience handling confidential laboratory and scientific dataExperience executing administrative strategiesExperience training staffKnowledgeKnowledge of the basic principles of biology, immunology and chemistryKnowledge of the principles of safe handling of potentially pathogenic substances and contaminated materialsKnowledge of CCAC and OMAFA regulationsFamiliar with the following acts and regulations: ISO 17025 (2017), OECD Principles on GLP, CCAC guidelines and policies and the Animals for Research ActKnowledge of occupational health and safety practicesKnowledge of the basic principles of scientific researchKnowledge and understanding of TPC's Standard Operating ProceduresKnowledge of computers, including word processing, spreadsheets and databasesStrong interpersonal and conflict resolution skills are essential for successfully engaging with diverse personalities and navigating complex workplace dynamicsDisclaimerAs part of our recruitment process, we may use digital or artificial intelligence–enabled tools to assist with tasks such as résumé screening, skills matching, or scheduling. These tools do not make final hiring decisions. All employment decisions are made by people.We are committed to fair, inclusive, and bias‐aware hiring practices and comply with Ontario legislation. If you require accommodation at any stage of the recruitment process, please let us know.

📌 Rodent Associate Study Coordinator - 18 Month Contract (Centre Wellington)
🏢 Transpharmation
📍 Centre Wellington