Clinical Research Associate

3 months ago

Mississauga, Canada Profound Medical Full time

Our mission is to Profoundly change the standard of care by creating a tomorrow where clinicians can confidently ablate tissue with precision; a tomorrow where patients have access to safe and effective treatment options, so they can quickly return to their daily lives. Changing the standard of care is part of our fabric. We are a group of energetic, problem-solvers focused on innovation, and looking to change the world. We are changing the paradigm for treating diseases such as prostate cancer by using real-time MR Imaging, thermal ultrasound and close-loop temperature feedback control, to gently ablate the diseased tissue with mínimal side effects.

If you share our values and want to work in a collaborative results focused culture and want to make a Profound impact in healthcare and your career, here is your chance.

**_ **Please note this is a 1 year contract position._**

**General Accountability**:
The CRA is a key member of the clinical trials team dedicated to achieving and exceeding business objectives through efficient execution, high quality and timely delivery of all associated aspects of clinical trial operations from startup to closeout.

**Duties and Responsibilities**:

- Participate in review of site contracts, budgets, and ethics board submissions.
- Establish relationship with study site personnel.
- Establish and maintain the Trial Master File ensuring copies of study documents including protocols, ethics approvals, patient-facing materials and site training and qualification are current and compliant.
- Ensure the study conduct, trial master file (TMF) and adverse event reporting are compliant with the ethics board approval, Good Clinical Practice (GCP) guidelines and applicable regulatory requirements.
- Ensure study data are accurate, complete, and verifiable through source data review/verification (SDR/SDV) and case report form (CRF) review as applicable, by on-site and remote monitoring activities. Resolve any discrepancies using Query Process.
- Gather analytics on clinical trial progress to ensure integrity of data collection and track project milestones.
- Perform site initiation visits, interim monitoring visits and close-out visits as needed.
- Provide support to Senior Clinical Management Team.
- Conduct training for colleagues or study team as requested.
- Fulfill other duties as required, including but not limited to tracking inventory and supplying study sites, and coordinating eligibility reviews.

**Education and Certification**:

- Bachelor's degree in health or medical sciences such as nursing, Master's degree preferred
- Diploma or certificate in clinical research or > 3 years of professional experience in a Clinical Research Associate role

**Key Attributes (experience, skills and technical knowledge)**:

- Proven experience in administering and conducting clinical trials from startup to closeout.
- Proficiency in Good Clinical Practice (GCP) guidelines, ethics board policies, applicable regulatory requirements and all related processes
- Proven ability to establish and maintain relationships with study site personnel.
- Proficiency in data management and quality management.
- Knowledge of adverse event reporting procedures and applicable regulatory requirements.
- Experience in conducting site initiation visits, monitoring visits, and close-out visits, both on-site and remotely.
- Outstanding interpersonal and communication skills
- Ability to manage multiple tasks simultaneously, track project milestones, and ensure timely delivery of results.
- Strong attention to detail
Strong ability to work both independently and collaboratively.

  • Clinical Research Coordinator

    3 months ago

    Mississauga, Canada Cliantha Research Ltd. Full time

    _Cliantha Research Inc._ is currently seeking Part-Time Clinical Research Coordinator(s) who can fulfill its business needs and is looking for better learning and growth opportunities. About Us Cliantha Research is a full service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase,...

  • Clinical Research Coordinator

    7 months ago

    Mississauga, Canada Cliantha Research Ltd. Full time

    _Cliantha Research Inc._ is currently seeking Part-Time Clinical Research Coordinator(s) who can fulfill its business needs and is looking for better learning and growth opportunities. About Us Cliantha Research is a full service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase,...

  • Clinical Training Supervisor

    3 months ago

    Mississauga, Canada Cliantha Research Ltd. Full time

    _Cliantha Research Inc._ is currently seeking a Full-time **Clinical Training Supervisor**; who can fulfill its business needs and is looking for better learning and growth opportunities. **About Us** Cliantha Research Inc. is a full service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late...

  • Clinical Advisor

    4 months ago

    Mississauga, Canada Clinical Research Dental Full time

    **Position Summary** This particular role is for an already established Territory in the Mississauga, Oakville, Acton, Cambridge, Georgetown and Milton, ON Region. ABOUT OUR ROLE: Our **Clinical Advisor** (Dental) is an exciting role accountable for developing sales and providing education within the assigned territory consistent with strategic and...

  • Clinical Research Associate

    4 months ago

    Mississauga, Canada AstraZeneca Full time

    **Role Overview**: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a...

  • Clinical Operations Supervisor

    3 months ago

    Mississauga, Canada Cliantha Research Ltd. Full time

    Job description **Job Description / Roles and Responsibilities for Job Title**: **1) **Assist Associate Director in supervising workload, productivity and work quality of staff, ensuring assigned tasks are completed accurately and within defined performance expectations. Other duties include, but are not limited to: **i. **Supervise performance and...

  • Clinical Systems Specialist

    6 months ago

    Mississauga, Canada Cliantha Research Full time

    Cliantha is currently seeking a **Clinical Systems Specialist **who can fulfill its business needs and is looking for better learning and growth opportunities. **About Us** Cliantha Research is a full service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Tobacco Research,...

  • Senior Project Coordinator for Clinical Research Operations

    2 weeks ago

    Mississauga, Ontario, Canada Pharma Medica Research Inc. Full time

    We are seeking a highly organized and detail-oriented Senior Project Coordinator to join our team at Pharma Medica Research Inc.About UsWe are a Contract Research Organization (CRO) dedicated to delivering high-quality research in the pharmaceutical industry. Our innovative approach and commitment to excellence have earned us a reputation as a trusted...

  • Clinical Research Professional

    2 weeks ago

    Mississauga, Ontario, Canada GlaxoSmithKline Full time

    Company Overview:GlaxoSmithKline is a leading pharmaceutical company dedicated to discovering and developing innovative treatments for patients worldwide.We are seeking highly motivated individuals to join our team as Clinical Study Associate Interns. This role offers an excellent opportunity to gain hands-on experience in clinical research and contribute to...

  • Clinical Research Associate

    6 months ago

    Mississauga, Canada AstraZeneca Full time

    **Clinical Research Associate - Biopharm** **Greater Toronto Area (Field based)** **12 Month Contract** At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation - ultimately providing employees with the opportunity to work across teams, functions and even the globe. Our...

  • Part-time Clinical Assistant

    6 months ago

    Mississauga, Canada Cliantha Research Ltd. Full time

    _**INSTRUCTION TO APPLY; PLEASE APPLY ACCORDINGLY OR YOUR APPLICATION WILL NOT BE ACCEPTED**:_ Cliantha is currently seeking **Part Time Clinical Assistant(s)**; who can fulfill its business needs and is looking for better learning and growth opportunities. **About Us** Cliantha Research is a full service Clinical Research Organization (CRO) that provides...

  • Clinical Content Specialist, Regulatory Documents

    6 days ago

    Mississauga, Ontario, Canada Pharma Medica Research Inc. Full time

    We are a full-service contract research organization dedicated to delivering innovative solutions in the highly regulated pharmaceutical industry.Our ideal candidate will have expertise in researching regulatory guidelines and generating high-quality study-related materials and documents. The successful Associate Medical Writer will work closely with our...

  • Associate Director

    7 months ago

    Mississauga, Canada AstraZeneca Full time

    **Job Title: Associate Director Clinical Coding**: **Career Level - E** **Introduction to Role**: Are you ready to take the next step in your career? As an Associate Director of Clinical Coding, you will be at the forefront of overseeing clinical coding for ongoing clinical studies with medium scope and complexity. You will be responsible for the delivery...

  • Clinical Content Specialist

    1 week ago

    Mississauga, Ontario, Canada Pharma Medica Research Inc. Full time

    Job Title: Clinical Content SpecialistWe are seeking an experienced and detail-oriented Clinical Content Specialist to join our team at Pharma Medica Research Inc.About Us:Pharma Medica Research Inc. is a Contract Research Organization dedicated to delivering high-quality clinical trials services in a highly regulated industry.Estimated Salary Range: $80,000...

  • Clinical Documentation Specialist

    1 week ago

    Mississauga, Ontario, Canada Pharma Medica Research Inc. Full time

    Job SummaryWe are seeking a highly skilled Clinical Documentation Specialist to join our team at Pharma Medica Research Inc.About UsPharma Medica Research Inc. is a Contract Research Organization that specializes in conducting early phase clinical trials. We are committed to innovation and original solutions in a highly regulated industry.Key...

  • Senior Laboratory Research Associate

    2 weeks ago

    Mississauga, Ontario, Canada Vitalbio Full time

    Vitalbio is a dynamic and innovative company that empowers scientists to create life-changing solutions.Estimated salary range for this position: $80,000 - $110,000 per year.About the Role:We are seeking a highly skilled Laboratory Research Associate to join our team of passionate researchers. This role will play a critical part in driving the development of...

  • Associate Medical Writer, Regulatory

    2 weeks ago

    Mississauga, ON, Canada Pharma Medica Research Inc. Full time

    Pharma Medica Research (PMRI) is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. We are a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are currently looking for an ...

  • Associate Medical Writer

    2 weeks ago

    Mississauga, Canada Pharma Medica Research Inc. Full time

    Pharma Medica Research (PMRI) is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. We are a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are actively looking for...

  • Associate Medical Writer

    2 weeks ago

    Mississauga, Canada Pharma Medica Research Inc. Full time

    Pharma Medica Research (PMRI) is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. We are a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are actively looking for...

  • Associate Medical Writer

    2 weeks ago

    Mississauga, Canada Pharma Medica Research Inc. Full time

    Pharma Medica Research (PMRI) is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. We are a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are actively looking for...