Central Monitoring Manager

Posted Yesterday
Be an Early Applicant
Hiring Remotely in Vilnius, Vilniaus apskritis, LTU
In-Office or Remote
77K-77K Annually
Entry level
Pharmaceutical
The Role
Leads risk-based and centralized monitoring activities for clinical studies, ensuring patient safety and data integrity. Responsibilities include study risk management, RBM platform implementation, review of risk indicators and statistical analyses, targeted source data verification, central data review, reporting findings to clients and study teams, and developing monitoring plans. The role also supports proposals and collaborates with Clinical Data Science on data-driven solutions.
Summary Generated by Built In
Company Description

PSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

    Job Description

    With the industry moving forward, the central monitoring function has become a top priority at PSI. We are looking for a person, who would lead the risk-based monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.

    You will:

    • Lead and facilitate initial and ongoing study Risk Management
    • Participate in selection and setup of the RBM platform
    • Perform Centralized Monitoring for a study including review of Key Risk Indicators, Statistical Analyses and Quality Tolerance Limits
    • Present Centralized Monitoring analysis results to study teams and clients and manage issues in cross-functional environment
    • Develop and review study-specific Plans
    • Set up and manage targeted SDV and monitoring strategy for a study
    • Set up and manage Central Data Review activities in a study
    • Contribute to Proposals and bid defense meetings with information about Risk Based Monitoring services
    • Communicate study challenges to Clinical Data Science group and work out data-driven solutions

    Qualifications

    • College/University degree or an equivalent combination of education, training and experience
    • Clinical Study Lead/Manager experience
    • Strong communication & presentation skills are essential
    • Leadership and ability to work independently are essential
    • Centralized Monitoring experience is a plus
    • Critical thinking and analytical skills
    • Ability to work with complex data and provide insight into risk reports and trends
    • Ability to adapt to changing circumstances and learn quickly
    • Knowledge of the process and functions in clinical trials, ability to understand the protocol and study associated risks
    • Full working proficiency in English (Lithuanian proficiency is a plus)
    • Proficiency in MS Office applications, Excel skills

    Additional Information

    This role is not only important for every CRO, but it is booming now. This is an opportunity to work on a frontline of the industry, set the grounds for risk-based models and get a global helicopter view on each project.

    We offer:

    • Excellent working conditions
    • Extensive training and friendly team
    • Opportunities for personal and professional growth
    • A fair and attractive salary and benefits package starting at EUR 77.000 gross. The precise salary depends on the specific qualifications and experience, and will be agreed upon on an individual basis.

    Skills Required

    • College or university degree, or equivalent combination of education, training, and experience
    • Clinical Study Lead or Clinical Study Manager experience
    • Strong communication and presentation skills
    • Leadership ability and capacity to work independently
    • Critical thinking and analytical skills
    • Ability to work with complex data and provide insight into risk reports and trends
    • Ability to adapt to changing circumstances and learn quickly
    • Knowledge of clinical trial processes and functions, including protocol and study risk assessment
    • Full working proficiency in English
    • Proficiency in Microsoft Office applications and Excel
    • Lithuanian proficiency
    • Centralized Monitoring experience
    Am I A Good Fit?
    beta
    Get Personalized Job Insights.
    Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

    The Company
    HQ: Zug
    1,939 Employees
    Year Founded: 1995

    What We Do

    PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

    Similar Jobs

    Remote
    6 Locations
    20524 Employees
    In-Office or Remote
    Vilniaus miesto, Vilnius, Vilniaus apskritis, LTU
    28 Employees
    28-40 Hourly
    In-Office or Remote
    Vilniaus miesto, Vilnius, Vilniaus apskritis, LTU
    28 Employees
    30-40 Hourly

    Modash Logo Modash

    Data Engineer

    Marketing Tech • Software
    In-Office or Remote
    6 Locations
    56 Employees

    Similar Companies Hiring

    Formation Bio Thumbnail
    Artificial Intelligence • Big Data • Healthtech • Biotech • Pharmaceutical
    New York, NY
    150 Employees
    Pfizer Thumbnail
    Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
    New York, NY
    121990 Employees
    Cencora Thumbnail
    Healthtech • Logistics • Pharmaceutical
    Conshohocken, PA
    51000 Employees

    Sign up now Access later

    Create Free Account

    Please log in or sign up to report this job.

    Create Free Account