Manager, Clinical Data Scientist, Clinical Data Sciences

2 weeks ago

Kirkland, Canada Pfizer Full time

Use Your Power for Purpose

At Pfizer, our mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. You will play a pivotal role in improving patients' lives by ensuring the accuracy, timeliness, and consistency of clinical data. Your work will bridge evidence-based medical decision support with colleagues and stakeholders, enhancing health and treatment outcomes. By developing robust frameworks, providing unbiased expertise, and addressing data gaps, you will contribute to better health outcomes and the safe use of medicines. Your dedication will help Pfizer achieve new milestones and support patients worldwide.

What You Will Achieve

In this role, you will:

- Lead and manage people, technology, and financial resources within the department.
- Actively share knowledge and identify potential improvements in processes or products, taking risks to develop innovative ideas.
- Solve moderately complex problems within your expertise and assist with issues outside the department.
- Oversee operational activities to support the department's short-term goals and manage the performance of direct reports through goal setting, coaching, and ongoing assessment.
- Recognize the need for development in others, collaborate to create development plans, and solicit input to explain complex concepts and persuade others.
- Process, review, and receive patient data and records, ensuring accurate, timely, and consistent clinical data reaches the medical department and other groups.
- Develop data management plans, including data preparation and validation activities, and guide operational teams in managing projects and identifying areas for improvement.
- Facilitate agreements between different teams, taking a leadership role, and serve as a Clinical Data Scientist and Trial Lead for clinical trials.
- Act as a technical resource to study teams for data visualization and reporting tools, ensuring operational excellence in collaboration with partners.
- Perform central monitoring activities, plan and execute communication strategies, and engage customer populations effectively.

Here Is What You Need (Minimum Requirements)
- BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate's degree with at least 8 years of experience or high school diploma (or equivalent) with at least 10 years of relevant experience
- Comprehensive understanding of all phases of clinical trials
- Familiarity with clinical research, FDA regulations, and International Conference on Harmonization Good Clinical Practices (GCDMP)
- Strong project and risk management skills
- Excellent verbal and written communication abilities
- Capability to handle multiple tasks and projects efficiently

Bonus Points If You Have (Preferred Requirements):

- Master's degree
- Contract Research Organization (CRO) and vendor oversight experience
- Proficient in using commercial clinical data management systems and/or EDC products
- Ability to adapt to changing priorities and manage multiple projects simultaneously
- Strong interpersonal skills and the ability to build relationships with stakeholders

Other Job Details:

- Eligible for Employee Referral Bonus
- Not Eligible for Relocation Assistance

Work Location Assignment: Hybrid

At Pfizer, we embrace diversity and inclusion for innovation and growth. We are committed to building inclusive teams and an equitable workplace for our employees to bring their true selves to work.

Chez Pfizer, nous accueillons la diversité et l'inclusion pour stimuler l'innovation et la croissance. Nous sommes déterminés à créer des équipes inclusives et un milieu de travail équitable pour que nos employés puissent exprimer leur vraie personnalité au travail.

Medical

LI-PFE

  • Manager, Clinical Data Scientist, Clinical Data

    2 weeks ago

    Kirkland, Canada Pfizer Full time

    ROLE SUMMARY As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Clinical Data Scientist (CDS) is responsible for timely and high-quality data management deliverables supporting the Pfizer portfolio. The CDS delivers asset level information strategies...

  • Clinical Research Associate- Sponsor Dedicated

    3 weeks ago

    Kirkland, Canada Novasyte Full time

    Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

  • Contract Clinical Research Associate, Oncology

    7 days ago

    Kirkland, Canada Novasyte Full time

    IQVIA Biotech is seeking a part-time Contract Sr. CRA with Oncology monitoring experience. Must be based in Eastern Canada. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest...

  • Bilingual Clinical Trial Coordinator

    2 weeks ago

    Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of...

  • Bilingual Clinical Trial Coordinator

    4 weeks ago

    Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration:Track (e.g. essential documents) and report (e.g. Safety Reports)Ensure collation and distribution of study tools...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    Kirkland, Quebec, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration:Track (e.g. essential documents) and report (e.g. Safety Reports)Ensure collation and distribution of study tools...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: - Track (e.g. essential documents) and report (e.g. Safety Reports) - Ensure collation and distribution...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of study...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Clinical Trial Coordinator (CTC)Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of study...

  • Statistical Expert for Clinical Trials

    2 days ago

    Kirkland, Quebec, Canada IQVIA LLC Full time

    **Job Overview:**IQVIA LLC is seeking a highly skilled Statistical Expert to support our clinical trials. As a key member of our team, you will provide statistical input to study synopses and protocols, collaborate with project teams to establish project timelines, and manage internal and CRO project activities.Responsibilities:Collaborate with...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of...

  • Bilingual Clinical Trial Coordinator

    4 weeks ago

    Kirkland, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration:Track (e.g. essential documents) and report (e.g. Safety Reports)Ensure collation and distribution of study...

  • Manager, Information Management

    5 days ago

    Kirkland, Canada Pfizer Full time

    Status : Regular, Full-Time Statut : Régulier, temps plein (Français à suivre) Global Product Development (GPD) supports clinical development across Pfizer and late-stage development of medicines. Every year, GPD partners with thousands of global participants, health systems and HCPs in our work to bring new medicines to market for the patients that we...

  • Chef d'équipe de données

    4 weeks ago

    Kirkland, Quebec, Canada IQVIA Argentina Full time

    Job Overview- Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet...

  • Clinical Trial Oversight Specialist

    1 day ago

    Kirkland, Quebec, Canada Pfizer Full time

    Job OverviewWe are seeking an experienced professional to join our team as the Clinical Trial Oversight Specialist. In this role, you will be responsible for leading activities to protect Pfizer from reputational risk resulting from the conduct of work/collaboration with HCPs and Clinical Trial Sites/Organizations.About the Team:The Site Intelligence,...

  • Director of Clinical Project Management

    7 days ago

    Kirkland, Canada Novasyte Full time

    Director, Global Project Leadership IQVIA’s Directors within Global Project Leadership direct and manage the team responsible for clinical delivery of complex; global full service, multi-regional studies and/or programs as well as strategic decision-making responsibility for the project/program. You will hold responsibility for the direction and...

  • Senior Biostatistician for Data Analysis

    2 days ago

    Kirkland, Quebec, Canada IQVIA LLC Full time

    **Job Description:**We are seeking a highly experienced Sr. Biostatistician to join our team at IQVIA LLC. As a key member of our team, you will provide statistical support for drug development programs in phases 2 or 3 with efficacy and safety endpoints.Key Responsibilities:Collaborate with multidisciplinary project teams to establish project...

  • Bilingual Clinical Trial Coordinator

    4 weeks ago

    Kirkland, QC, Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration: Track (e.g. essential documents) and report (e.g. Safety Reports) Ensure collation and distribution of...

  • Bilingual Clinical Trial Coordinator

    3 weeks ago

    montréal (kirkland), Canada ICON Strategic Solutions Full time

    As a Clinical Trial Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing: Clinical Trial Coordinator (CTC) Trial and site administration:Track (e.g. essential documents) and report (e.g. Safety Reports)Ensure collation and distribution of study...