Register
Recruit Create CV

Clinical Trial Manager Ii Jobs

Project Manager Ii Jobs
By Hayleys Advantis Limited LLC. At Canada
3+ years of experience in project/program management
2+ years of experience with data governance; audit & performance management experience strongly preferred
Strong analytic skills and a demonstrated ability to build and manage data management processes
Undergraduate degree in analytics, data science, business, finance, engineering, or a related field.
1+ years of experience in ESG and sustainability reporting
Fluency in standard software including MS Excel. Knowledge of SQL is a strong plus.
Senior Regional Clinical Trial Manager - Fully Remote Us Or Canada
By ICON Strategic Solutions At Canada
Responsible for Study Management and oversight of all Study Management functions internally and at the CROs
2+ years’ experience as a clinical Study, Trial or Project Manager.
Study Manager experience must be from Pharma, biotech or a CRO.
• Company value: (Senior Management, Culture & Values, Diversity & Inclusion)
Lead and manage the tactical execution of one or more clinical studies from study startup through database release.
Drive decision making and work closely with the Clinical Project Manager to provide input to operational strategy
Field Trial Manager Jobs
By Loam Bio At Calgary, Alberta, Canada
Experience in field trial management and/or agronomy
Strong communication, leadership, and project management skills
Knowledge of Canadian broadacre cropping systems
Experience in the design of agricultural experiments
Experience in data analysis and statistical methods
Competitive salary based on experience
Clinical Data Analyst Ii
By Premier Research At Canada
2-5 years Relevant experience in clinical research or related fields (Site-Operations, Monitoring On-site/Remote, Data Management, Hospital settings), global study experience, preferred.
Ability to use analytical tools to extracting knowledge and insight from data (data mining)
In-depth knowledge of ICH/GCP regulations FDA Guidance Documents, EU Directives
In-depth knowledge of clinical monitoring procedures
We are Built by You. Your ideas influence the way we work, and your voice matters here.
Develops Risk Analytics Monitoring Plan for assigned studies
Clinical Trial Coordinator Jobs
By Fortrea At Montreal, Quebec, Canada
Good organizational and time management skills
Manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines.
Facilitate translation and back translation of all necessary documents as appropriate for local country requirements and as needed regionally.
Good communication skills, oral and written
Monitor site performance and implement action plans for sites not meeting expectations, in conjunction with the CRA.
Assist with the coordination of study visits and shipment of drug, ancillary supplies and laboratory kits/samples.
Senior Local Trial Manager (Remote) (Canada) (Clinical)
By ICON Strategic Solutions At Canada
Advanced: 3 to 5+ years of trial management experience.
The efficient management of local vendors
Proactive risk management and budget forecasting
Timely review of trip reports submitted by Site Managers
A minimum of a 4-year Bachelor’s degree or relevant clinical experience is required
At least 2 years of Oncology experience required
Manager Operations Ii Jobs
By Cadillac Fairview At Montreal, Quebec, Canada
Minimum 10 years experience in Physical Operations management with at least 7 years supervisory/management experience preferably in a mixed use environment
Thorough knowledge of: general maintenance procedures, budgeting principles, electrical and practical theory, new technologies, HVAC, electrical/mechanical systems, management principles, budgeting principle
CFM ( Certified Facilities Manager) certification is an asset
Proven leadership abilities and self starter( Proven leadership skills in a progressive company)
Good organizational skills and ability to manage multiple tasks and prioritize for completion
Ensure that all preventative maintenance requirements for all mechanical/electrical system and equipment is evaluated/documented and performed;
Clinical Psychologist Ii [Nl Health Services]
By CareerBeacon At Gander, Newfoundland and Labrador, Canada
Strong skills in interpersonal relationships, interdisciplinary team collaboration, leadership, communication, advocacy, networking, time management, case management and client support.
Significant (2-5 years) and current (within the last 5 years) experience in a mental health and/or addictions setting.
Experience working with individuals, families and groups.
Demonstrated knowledge of program, services and community resources.
A strong knowledge of psychological interventions and the DSM-5
Functions with a high level of autonomy while functioning as a member of an interdisciplinary team.
Project Manager Ii Jobs
By Astek Canada At Toronto, Ontario, Canada
SUMMARY OF DAY TO DAY RESPONSIBILITIES:
• Ensures change process and documentation is effectively managed, communicated, and tracked to completion with segment partners
• Manage production implementation with teams/stakeholders during change window
2.) Infrastructure experience (servers, firewalls, migration) – 3 years
3.) Experience with Agile methodology – 3 years
4.) Jira experience – 3 years
Operations Manager Ii Jobs
By DHL Supply Chain At Mississauga, Ontario, Canada
2-4 years of experience in a supervisory or management role, required
Experience with P&L management, objective setting and project management, required
You’ll manage multiple areas with multiple priorities and multiple stakeholders – every day
You’ll support your team’s development through the endless learning opportunities DHL Supply Chain offers
You won’t be micro-managed by your General Manager – but you will be held accountable
You’ll learn, grow, and become the type of manager you’d like to work for
Clinical Trial Operations Specialist
By System One At Toronto, Ontario, Canada
Planning, coordination and conduct of complex, regulatorily defined tasks
Seamless trial operation and communication to all applicable stakeholders
Timely delivery of all the materials, documentation and information needed to setup, execute, and delivery of the assigned trial(s)
Overnight of trial supplies, documentation, submissions, and other operational parameters
Clinical Trial Assistant Jobs
By ICON Strategic Solutions At Canada
At least 2 years of related experience
Bachelor’s Degree preferred in scientific/medical discipline or equivalent experience.
Experience with clinical trials required
Experience with study start-up, maintanance, close-out of clinical studies
Demonstrated expertise and experience Clinical Trial Coordination
Ability to maintain Clinical Trial Tracking systems.
Account Manager Ii Jobs
By Flexport At Greater Toronto Area, Canada
Collaborate globally with counterparts in Asia, Europe and Latin America, to ensure a consistent account management experience.
5+ years of experience in a sales/account management or a client facing role.
Deliver Unmatched Experience To Users
Worried about not having any logistics experience?
Cultivate and grow relationships with key business stakeholders that empower the client and deepen the relationship with Flexport.
Keep a pulse on account health and identify opportunities to upsell, cross-sell to ensure client success is met.
Clinical Trial Coordinator Jobs
By Parexel At Canada
Effective time management, organizational and interpersonal skills, conflict management.
Clinical supply & non‐clinical supply management, in collaboration with other country roles.
Manage Labeling requirements and coordinate/sign translation change request.
Minimum 1-2 years in Clinical Research or relevant healthcare experience. Note - Specific experience requirements may vary depending on the Country
Maintenance of tracking tools. o Working knowledge of contract development, negotiation, approval, and maintenance (e.g., Clinical Trial Research Agreements (CTRAs)).
Completes training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, and system and process related training.
Product Manager Ii Jobs
By Seismic At Toronto, Ontario, Canada
3-4 years of proven software Product Management experience
Proven analytical skills and experience using data to drive decision-making and feature prioritization
Develop specifications, negotiate & define scopes, and partner with our design & engineering teams to deliver new capabilities to our customers
Bachelor's degree in Computer Science, Business Systems, similar technical field of study, or equivalent practical experience
Product taste - you have a demonstrated passion for user experience and have delivered software that delights users
Excellent verbal, visual, and written communication skills
Clinical Trial Coordinator Jobs
By Source Nutraceutical, Inc. At Winnipeg, Manitoba, Canada
Knowledge and/or experience in working with Clinical Trial Management System (CTMS), e-consent processes, e-data collection (EDC), and storage.
Experience working with project management software.
Knowledge and experience in ICH/GCP and Good Documentation Practice (GDP).
Additional education and/or professional certifications would be an asset, including:
Certified Associate of Project Management (CAPM).
The ability to analyze, organize, prioritize, and manage multiple projects.
Clinical Trial Coordinator - Regulatory - Montreal
By ICON Strategic Solutions At Montreal, Quebec, Canada
Completed job training (office management, administration, finance, health care preferred) or B.A./B.S. (Life Science preferred) or equivalent healthcare experience
Highly effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request
Excellent negotiation skills for CTCs in finance area
Minimum 1-2 yrs in Clinical Research or relevant healthcare experience
Clinical Trial Coordinator /Cta Montreal
By ICON Strategic Solutions At Canada
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request
Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:
Track (e.g. essential documents) and report (e.g. Safety Reports)
Ensure collation and distribution of study tools and documents
Update clinical trial databases (CTMS) and trackers
Project Manager Ii Jobs
By TELUS At Vancouver, British Columbia, Canada
Bachelor’s degree or post-secondary diploma or equivalent education and/or program management experience is required / preferred
2-3 years of project management experience, project plan creation and change management principles, leading to successful execution
Project Management: Independently coordinate work with clinical care teams to implement our service roadmap, managing schedules, and removing roadblocks
Communication: focus on facilitating discussions across teams, including executives, and creating an environment that supports ideas, sharing and knowledge sharing
1+ years of relevant experience in healthcare or private clinics environments
Easy access to a broad range of services in preventive health, wellness, mental health and occupational health
Administrative Assistant Ii, Clinical Engineering
By IWK Health At Halifax, Nova Scotia, Canada
Experience inputting database information and managing a Computerized Maintenance Management System(CMMS) is preferred, Knowledge in Megamation Systems ‘DirectLine’ is an asset.
Proven time management, organizational, and problem-solving skills required
Minimum six (6) months related administrative/secretarial experience, ideally in a health care environment, required.
Advanced working knowledge of computers including Windows and Microsoft Office (Outlook , Excel, Word, PowerPoint, and Teams)
Keyboarding skills of 60 wpm required.
Experience with payroll entry and/or SAP an asset.

Are you looking for an exciting opportunity to manage clinical trials and help bring life-saving treatments to patients? We are seeking a Clinical Trial Manager to join our team and help lead our clinical trials to success. If you have a passion for research and a commitment to excellence, this could be the perfect job for you!

Overview A Clinical Trial Manager is responsible for the successful management and execution of clinical trials. They are responsible for the coordination of all aspects of the trial, including the development of the protocol, the selection of sites, the recruitment of participants, the collection of data, and the analysis of results. Detailed Job Description A Clinical Trial Manager is responsible for the successful management and execution of clinical trials. They are responsible for the coordination of all aspects of the trial, including the development of the protocol, the selection of sites, the recruitment of participants, the collection of data, and the analysis of results. They must ensure that the trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). They must also ensure that the trial is conducted in a timely and cost-effective manner. Job Skills Required
• Knowledge of clinical trial regulations and GCP
• Excellent organizational and project management skills
• Ability to work independently and as part of a team
• Excellent communication and interpersonal skills
• Ability to manage multiple tasks and prioritize effectively
• Ability to work under pressure and meet deadlines
• Knowledge of medical terminology
• Knowledge of data management systems
Job Qualifications
• Bachelor’s degree in a related field
• At least 5 years of experience in clinical trial management
• Certification in clinical research (e.g. CCRA, CCRP)
Job Knowledge
• Knowledge of clinical trial regulations and GCP
• Knowledge of medical terminology
• Knowledge of data management systems
Job Experience
• At least 5 years of experience in clinical trial management
Job Responsibilities
• Develop and implement clinical trial protocols
• Select and manage clinical trial sites
• Recruit and manage clinical trial participants
• Collect and analyze clinical trial data
• Monitor clinical trial progress
• Ensure compliance with applicable regulations and GCP
• Prepare and submit clinical trial reports
• Manage clinical trial budgets