Sr. Clinical Trial Manager – Magazica Career Hub

Title: Sr. Clinical Trial Manager

Company: Syneos Health
Location: Toronto, Ontario
Job Type: FlexTime, FullTime

Description:

This job posting is for a Senior Clinical Trial Manager position at Syneos Health, a biopharmaceutical solutions organization. The role involves overseeing site management, clinical monitoring, and central monitoring deliverables to ensure patient safety, protocol compliance, and data integrity. Responsibilities include identifying risks, proposing risk mitigations, coordinating training, overseeing resourcing allocations, and interacting with clients and other functional departments.

Qualifications for this role include a Bachelor's degree or RN in a related field, demonstrated leadership abilities, international work experience, expertise in site management and monitoring, and knowledge of Good Clinical Practice guidelines. Strong computer skills, conflict resolution abilities, and critical thinking skills are also required. Moderate travel may be necessary.

Job Responsibilities:

Oversee site management, clinical monitoring, and central monitoring deliverables

Review study scope, budget, and protocol content

Employ strategic thinking and problem-solving skills

Serve as an escalation point for communications with investigator site staff

Coordinate with other functional leaders to meet study milestones

Develop and maintain clinical study tools and templates

Coordinate training for the study team

Review project oversight dashboards and clinical trial systems

Interact with clients and other functional departments

Provide feedback on staff performance

May be assigned to larger, more complex trials

May coach and mentor CTMs regarding functional clinical delivery

Qualifications:

Bachelor's degree or RN in a related field

Demonstrated ability to lead and align teams

Experience in an international environment

Expertise in site management and monitoring

Knowledge of Good Clinical Practice guidelines

Strong computer skills

Strong conflict resolution skills

Demonstrated critical thinking skills

Moderate travel may be required

Overall, this role requires a candidate with strong leadership, communication, and problem-solving skills to ensure the successful management of clinical trials and deliverables at Syneos Health.

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Title: Sr. Clinical Trial Manager
Company: Syneos Health
Location: Toronto, Ontario
Updated: Today   
Location: Toronto, ON, Canada   
Job ID: 25102803Description Sr. Clinical Trial ManagerSyneos HealthÂ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a FullService environment, youâll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Discover what our 29,000 employees, across 110 countries already know:WORK HERE MATTERS EVERYWHEREWhy Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
 We are committed to our Total Self culture â where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
 We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives â weâre able to create a place where everyone feels like they belong.

Job Responsibilities

Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT).
 Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/CeMs) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope.
 Employs strategic thinking and problemsolving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting.
 Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution.
 Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities.
 Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed. Ensures access and audit trail reviews are conducted as required.
 Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study.
 Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality. Ensures quality of the clinical monitoring, central monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools.
 Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency) according to plan.
 Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan. Is accountable for their assigned clinical team members' understanding, ongoing compliance and delivery according to the stated monitoring strategy, CMP/SMP, and risk plans.
 Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity. Document requested revisions and approvals in CTMS. Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines.
 Interacts with the client and other functional departments related to clinical monitoring, central monitoring and site management activities and deliverables. Provides status updates on the clinical deliverables and risks to clients, project management and leadership as per departmental or study agreements. Provides solutions for obstacles in protocol execution and site management.
 Demonstrates understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection Readiness for clinical trial management scope.
 Oversees CRAs and Central Monitors assigned to the study and routinely assesses studyspecific process and training compliance, CMP compliance, and identifies emerging risks. Develop and support execution of corrective action plans at site and study level. Supports and completes activities to achieve data cut and lock deadlines.
 Provides feedback to line managers on staff performance including strengths as well as areas for development.
 May be assigned to larger, more complex trials or may coordinate clinical activities for a team of CTMs across a portfolio of projects
 May coach and mentor CTMs regarding functional clinical delivery, evaluation of project risks, and action implementation.

Qualifications:

Bachelorâs degree or RN in a related field or equivalent combination of education, training, and experience
 Demonstrated ability to lead and align teams in the achievement of project milestones
 Demonstrated capability of working in an international environment.
 Demonstrated expertise in site management and monitoring (clinical or central)
 Preferred experience with riskbased monitoring
 Demonstrates understanding of clinical trial management financial principles and budget management
 Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
 Must demonstrate good computer skills
 Strong conflict resolution skills
 Demonstrated ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project.
 Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues
 Moderate travel may be required, approximately 20%

Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, youâll take the initiative and challenge the status quo with us in a highly competitive and everchanging environment. Learn more about Syneos Health.Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.Summary Roles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies at the organization's facilities. Collaborates with the principal investigator, liaisons between research subjects, client teams, investigators, and clinic operations teams, and plans logistics and resource usage. Tracks study progress in alignment with project milestones, client deliverables, and budget, and follows applicable regulations globally and by region. Impact and Contribution Includes executives as well as managers, supervisors and team leads providing strategic vision and/or tactical direction across a discipline and/or broader organization. The majority of time is spent overseeing their area of responsibility, planning, prioritizing, and/or directing the responsibilities of employees. Goal are achieved through management of process, policy, and performance of direct and/or indirect reports. Manages a team of individual contributors and/or Supervisors. Delivers operational results that have direct impact on immediate or shortterm department results. Indepth knowledge and skills within a scientific/technology or professional discipline, understanding impact of work on related areas. Requires practical knowledge in managing the execution of processes, projects and tactics within team.Share this job

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