Clinical Research Nurse Translational Research – AdventHealth – Orlando, FL

Company: AdventHealth

Location: Orlando, FL

Expected salary:

Job date: Fri, 30 May 2025 01:43:16 GMT

Job description:

Job Description: Clinical Coordinator

Location: Orlando, FL 32803

Community You’ll Be Caring For:
Join a vibrant and supportive community dedicated to enhancing the lives of our residents. Our facility is committed to providing exceptional care and fostering a welcoming environment where both staff and residents thrive. We believe in comprehensive wellness and are passionate about delivering high-quality services to our diverse population.

The Role You’ll Contribute:
As a Clinical Coordinator, you will play a crucial role in overseeing the clinical operations within our facility. You will ensure that all health and safety regulations are met while providing compassionate care to residents. Your responsibilities will include:

  • Developing and implementing individualized care plans in collaboration with nursing staff and other healthcare teams.
  • Conducting regular assessments and evaluations to monitor residents’ health status and adjust care plans as necessary.
  • Coordinating with multidisciplinary teams to facilitate effective communication and optimize patient outcomes.
  • Educating staff, residents, and families about health management, enhancing overall quality of care.
  • Maintaining accurate medical records and ensuring compliance with all regulatory requirements.
  • Participating in quality improvement initiatives and contributing ideas for enhancing facility operations.

Ideal candidates will have strong leadership skills, a commitment to high-quality patient care, and a passion for working with diverse populations. Join us in making a meaningful difference in the lives of those we serve!

Clinical Research Nurse Translational Research – AdventHealth – Orlando, FL

Company: AdventHealth

Location: Orlando, FL

Expected salary:

Job date: Thu, 22 May 2025 23:24:09 GMT

Job description:

Job Description: Clinical Research Nurse – RN/Associate

Marketing Statement:

Join our dynamic team as a Clinical Research Nurse – RN/Associate, where you’ll play a critical role in advancing healthcare through innovative clinical trials. In this rewarding position, you will collaborate with multidisciplinary teams to ensure the safe and effective conduct of clinical research studies, contributing directly to the improvement of patient outcomes.

The Role You’ll Contribute:

As a Clinical Research Nurse, you will be responsible for the recruitment, assessment, and monitoring of study participants, ensuring compliance with regulatory and ethical standards. You will utilize your clinical expertise in patient care to facilitate trial protocols while providing exceptional support to patients and their families throughout their research journey. Your contributions will help drive groundbreaking discoveries in medicine, making a direct impact on the future of healthcare.

Key Responsibilities:

  • Collaborate with research teams to implement and manage clinical trials
  • Conduct patient assessments and monitor study participants for safety and protocol adherence
  • Educate patients and their families about study requirements, potential risks, and benefits
  • Maintain accurate and timely documentation in accordance with regulatory guidelines
  • Support recruitment efforts and assist with data collection and analysis

Qualifications:

  • Currently licensed as a Registered Nurse (RN) in [state]
  • Experience in clinical research or related nursing fields preferred
  • Strong interpersonal and communication skills
  • Ability to work in a fast-paced, collaborative environment

Embark on a fulfilling career where your expertise makes a difference. Apply now to be part of our mission to advance clinical knowledge and improve patient care.

Translational Research in Oncology – Senior Clinical Quality Assurance Auditor – Toronto, ON

Company: Translational Research in Oncology

Location: Toronto, ON

Expected salary: $80000 – 110000 per year

Job date: Wed, 14 May 2025 06:45:40 GMT

Job description: If you are an experienced Senior Clinical Quality Assurance Auditor (internally referred to as Senior Clinical Quality Assurance Manager) who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO is seeking a Senior Clinical Quality Assurance Auditor (internally referred to as Senior Clinical Quality Assurance Manager) to join our Quality Assurance team. Reporting to the Senior Director of Quality Assurance, this position will be remote-based in Canada.Responsibilities: * Conduct Audits: Plan and execute comprehensive audits of clinical trials. This includes auditing clinical trial master files, internal processes, investigator sites, contract research organizations (CROs), and other relevant entities to assess compliance with relevant regulations, guidelines, and standard operating procedures (SOPs).

  • Host Audits/Inspections: Assist in hosting Sponsor audits and Regulatory Authority inspections. This includes providing support in coordinating the preparation and conduct of the audit/inspection, and in developing the responses (CAPA) to any findings,
  • Quality Assurance Documentation: Develop and maintain quality assurance documentation, including audit plans, audit reports, inspection readiness plans, and other relevant documents. Ensure accurate and timely documentation of audit findings, observations, and corrective actions taken.
  • Training and Education: Provide training and guidance to internal staff and external stakeholders on quality assurance practices, regulations, and industry standards related to clinical research. Foster a culture of quality and compliance through educational initiatives and ongoing support.

Quality Management System: Provide support in developing and maintaining the Quality Management System of the Organization, including support in the creation and revision of written procedures, conducting trending and metrics analysis for the QA activities * Process Improvement: Collaborate with cross-functional teams to identify areas for process improvement and develop strategies to enhance the efficiency and effectiveness of clinical quality systems. Implement best practices and drive continuous improvement initiatives.

  • Regulatory Compliance: Stay updated with current regulations, guidelines, and industry trends pertaining to clinical quality assurance. Interpret and communicate regulatory requirements to ensure compliance across clinical research activities.
  • Risk Assessment: Conduct risk assessments related to clinical quality assurance to identify potential vulnerabilities and areas of concern. Develop risk mitigation strategies and ensure appropriate controls are implemented.
  • Collaboration and Communication: Foster strong working relationships with internal stakeholders, including clinical operations, regulatory affairs, data management, and other departments. Collaborate effectively with external parties, such as auditors, regulatory authorities, and vendors, to facilitate audits, inspections, and regulatory submissions.

Requirements:

  • Bachelor’s degree in a relevant scientific field (such as life sciences, pharmacy, or nursing). A higher degree (Master’s or Ph.D.) is advantageous.
  • Minimum 5 experience in clinical quality assurance (8 preferred) , including conducting audits and inspections in the pharmaceutical, biotechnology, or clinical research organization (CRO) setting.
  • In-depth knowledge of applicable regulations and guidelines, such as Good Clinical Practice (GCP), International Council for Harmonisation (ICH), and relevant regional requirements (e.g., FDA, EMA).
  • Strong understanding of clinical trial processes, including study design, protocol development, data management, and adverse event reporting.
  • Excellent analytical and problem-solving skills, with the ability to critically evaluate complex data, identify trends, and propose effective solutions.
  • Demonstrated leadership abilities, including the ability to mentor and guide junior team members, and effectively collaborate with cross-functional teams.
  • Excellent communication skills, both written and verbal, with the ability to effectively communicate complex concepts and audit findings to various stakeholders.
  • Attention to detail, with a strong commitment to accuracy and quality in all work performed.
  • Relevant certifications, such as Certified Quality Auditor (CQA), Certified Clinical Research Professional (CCRP), or similar, are highly desirable.
  • Knowledge of risk-based quality management principles and experience with risk assessment methodologies is a plus.
  • Fluent oral and written English is required,
  • Intermediate proficiency in Word, Excel, and PowerPoint, is required.
  • Ability to travel worldwide (Europe, North America, Asia and occasionally in other locations), on an as-needed basis.

What TRIO Can Offer You:

  • Annual compensation review with opportunities for professional growth
  • 3 weeks of vacation plus paid December Holiday Closure
  • 10 days paid personal/sick time
  • 1 paid volunteer day / year
  • A rich benefit plan with Health, Dental, Vision & Life Insurance premiums paid by TRIO
  • Up to 5% RRSP Matching Program
  • Voluntary TFSA Program Available
  • Flexible working hours to promote work-life balance
  • Monthly Internet Allowance to support working from home
  • Work arrangement options (Office-Based/Hybrid/Home Based) with a one-time Home Office Allowance
  • Mobile Phone Stipend available for qualifying positions
  • Out-of-country Work: Employees can request to work internationally for a short period of time each year
  • Maternity / Parental Leave Top-Up Program
  • Employee Family Assistance Program to support you and your family during difficult times
  • Employee Recognition Program to reward long-term employees
  • Employee Referral Bonus Program

Pay Range: $80,000.00 to $110,000.00 – Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.Teamwork · Passion · Integrity · InnovationPowered by JazzHR

Translational Research in Oncology – Senior Clinical Research Associate – Toronto, ON

Company: Translational Research in Oncology

Location: Toronto, ON

Expected salary: $125000 – 142500 per year

Job date: Fri, 16 May 2025 00:13:56 GMT

Job description: If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO is looking for a Senior Clinical Research Associate to join our international team. Reporting to a CRA Line Manager, this position will be remote-based in CanadaResponsibilities:

  • Conducting site visits, including pre-study, initiation, monitoring and termination;
  • Confirming adherence to all FDA, ICH-GCP and local regulations;
  • Ensuring the completion and collection of regulatory documents;
  • Performing data verification of source documents;
  • Ensuring implementation and compliance with FDA, ICH-GCP guidelines;
  • Participating in budget negotiation and follow-up where applicable;
  • Assisting with data validation and query resolution;
  • Mentoring junior team members as required.

Qualifications:

  • Bachelor’s Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health

Science – or its international equivalent * Minimum 5 years of previous CRA experience

  • A minimum of 2 years of monitoring experience in oncology trials
  • An advanced level of oncology knowledge
  • Completion of a science-related Bachelor’s degree
  • Excellent knowledge of medical terminology and clinical monitoring process
  • Strong ICH-GCPs knowledge
  • Experience with clinical trial information systems
  • Ability to travel up to 60% on average
  • Must work both independently and in a team environment
  • Read, write and speak fluent English
  • Ability to mentor and train new/junior CRAs on-site in a positive and effective manner

What TRIO Can Offer You:

  • Annual compensation review with opportunities for professional growth
  • 3 weeks of vacation plus paid December Holiday Closure
  • 10 days paid personal/sick time
  • 1 paid volunteer day / year
  • A rich benefit plan with Health, Dental, Vision & Life Insurance premiums paid by TRIO
  • Up to 5% RRSP Matching Program
  • Voluntary TFSA Program Available
  • Flexible working hours to promote work-life balance
  • Monthly Internet Allowance to support working from home
  • Work arrangement options (Office-Based/Hybrid/Home Based) with a one-time Home Office Allowance
  • Mobile Phone Stipend available for qualifying positions
  • Out-of-country Work: Employees can request to work internationally for a short period of time each year
  • Maternity / Parental Leave Top-Up Program
  • Employee Family Assistance Program to support you and your family during difficult times
  • Employee Recognition Program to reward long-term employees
  • Employee Referral Bonus Program

Pay Range: $125,000.00 to $142,500.00 – Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.Teamwork · Passion · Integrity · InnovationTeamwork · Passion · Integrity · InnovationPowered by JazzHR

Translational Research in Oncology – Clinical Research Start-Up Trial Manager – Toronto, ON

Company: Translational Research in Oncology

Location: Toronto, ON

Expected salary: $60000 – 90000 per year

Job date: Sat, 05 Apr 2025 06:53:58 GMT

Job description: Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO is looking for two Start-Up Managers to join our Strategy and Clinical Collaborations team, reporting to the Clinical Start-Up Team Lead. These positions will be home-based or remote, depending on the successful applicant’s city of residence. Both positions are based in Canada. One position is full-time and permanent, while the other is a full-time, 1-year contract.Responsibilities:

  • Implementation of site identification process and selection activities according to trial specificities.
  • Preparation of submission packages including the preparation of patient documents and follow-up until country/site approvals are granted.
  • Preparation of site activation according to agreed standards, including but not limited to:
  • Logistic aspects (e.g. provision of study materials and documents, accesses to systems)
  • Compilation of documents required for activation (e.g. Site Activation Package)
  • Contract and Budget negotiation
  • Site training requirements
  • Coordination of site activation activities with all TRIO departments involved until hand over to Project Management team.
  • Identification and escalation of country or site level issues that could impact site activation timelines
  • Reporting regular status of activities (internally and externally)

Qualifications:

  • Scientific or medical background is highly recommended
  • Excellent knowledge of clinical research standards (incl. ICH-GCP)
  • 2 years of experience in clinical research activities including relevant experience in site activation (e.g. monitoring)
  • Ability to integrate to an international team and efficiently interact with colleagues
  • Excellent organizational skills are required to supervise multiple parallel projects
  • Computer literacy
  • Fluent in English

What we can offer you:

  • Annual compensation review with opportunities for professional growth
  • 3 weeks of vacation plus paid December Holiday Closure
  • 10 days paid personal/sick time
  • 1 paid volunteer day / year
  • Benefit plan with Health, Dental, Vision & Life Insurance premiums paid by TRIO
  • Up to 5% RRSP Matching Program
  • Voluntary TFSA Program Available
  • Flexible working hours policy to promote work-life balance
  • Monthly Internet Allowance to support working from home and a one-time Home Office Allowance
  • Maternity / Parental Leave Top-Up Program
  • Employee Family Assistance Program to support you and your family during difficult times

Pay Range $60,000.00 to $90,000.00 – Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.We thank all candidates for their interest; only those selected for an interview will be contacted.Teamwork · Passion · Integrity · InnovationPowered by JazzHR

Translational Research in Oncology – Data Manager – Toronto, ON

Company: Translational Research in Oncology

Location: Toronto, ON

Expected salary: $70000 – 80000 per year

Job date: Sat, 08 Mar 2025 08:24:47 GMT

Job description: Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO’s head office is in Edmonton, Alberta, Canada, with operations all throughout Canada, the USA, France, and Uruguay. TRIO is looking for a Data Manager to join our Data Management team. Reporting to the Associate Director, Data Management, this position will be remote based in Canada.Responsibilities:Reporting to the Manager, Data Management, the Data Manager will be responsible for the below:

  • Manage day to day operations of multiple clinical trials to ensure timelines and quality standards are met, under minimal supervision
  • Synthesize protocol and protocol amendments and translate into a Case Report Form
  • Perform database amendments based on the Case Report Form in Medidata Rave
  • Manage day to day operations of multiple clinical trials to ensure timelines and quality standards are met, under minimal supervision
  • Attend and provide status updates during Sponsor/Internal meetings for multiple trials
  • Manage the creation, revision and approval of the Validation Tools including formal testing, as required under minimum supervision
  • Contribute to the writing and maintenance of trial-related documentation (DMP, TWI, DTP, DTS, UGD, etc.…)
  • Consult with other departments as necessary to solve data or Validation Tool issues/needs
  • File documents in, and maintain, Section F of the electronic Trial Master File
  • Prioritize tasks in line with TRIO/Sponsor expectations and decisions across multiple trials
  • Ensure compliance to Standard Operating Procedures and Guidelines for trial-related activities
  • Contribute to the development of new processes and standards

Qualifications, Skills and Experience:

  • Bachelor’s Degree (preferably in a health-related field) or relevant experience in a health-related field
  • Combinations of education and experience will be considered
  • Excellent computer skills
  • At least 3 years’ experience with Medidata Rave
  • Ability to synthesize information and use intuition and experience to solve problems
  • Demonstrate exceptional attention to detail, accuracy and thoroughness
  • Excellent written and verbal communication skills including the ability to present numeric data effectively
  • Works well under pressure and can ensure smooth delivery of projects in a positive team environment

What we can offer you:

  • Annual compensation review with opportunities for professional growth
  • 3 weeks of vacation plus paid December Holiday Closure
  • 10 days paid personal/sick time
  • 1 paid volunteer day / year
  • Benefit plan with Health, Dental, Vision & Life Insurance premiums paid by TRIO
  • Up to 5% RRSP Matching Program
  • Voluntary TFSA Program Available
  • Flexible working hours policy to promote work-life balance
  • Monthly Internet Allowance to support working from home and a one-time Home Office Allowance
  • Maternity / Parental Leave Top-Up Program
  • Employee Family Assistance Program to support you and your family during difficult times

Pay Range $70,000.00 to $80,000.00 – Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.We thank all candidates for their interest; only those selected for an interview will be contacted.Teamwork · Passion · Integrity · InnovationPowered by JazzHR

Translational Research in Oncology – Clinical Research Start-Up Trial Manager – Vancouver, BC

Company: Translational Research in Oncology

Location: Vancouver, BC

Job description: future to the world of today. TRIO is looking for a Start-Up Manager to join our Strategy and Clinical Collaborations team… Coordination of site activation activities with all TRIO departments involved until hand over to Project Management team…
TRIO is seeking a Start-Up Manager to join their Strategy and Clinical Collaborations team. The role will involve coordinating site activation activities with all TRIO departments until handover to the Project Management team.
Position: Customer Service Representative

Location: Toronto, ON

Salary: $18.00 to $22.00 hourly

Job Type: Temporary

Our client is in need of a Customer Service Representative. The successful candidate will be responsible for providing exceptional customer service to clients and ensuring satisfaction with every interaction. This role requires strong communication skills, the ability to handle a high volume of calls and emails, and a friendly and professional demeanor. The ideal candidate will have previous customer service experience, excellent problem-solving skills, and be able to work well in a team environment. This is a temporary position with the potential for permanent placement for the right candidate. If you are passionate about customer service and are looking for an exciting opportunity, apply now!

Expected salary: $60000 – 90000 per year

Job date: Tue, 23 Jan 2024 23:39:35 GMT