drjobs Associate Director Statistical Programming

Associate Director Statistical Programming

Employer Active

1 Vacancy
The job posting is outdated and position may be filled
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Poli - Italy

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

TFS HealthScience is a leading global midsize Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full servicecapabilities resourcing and Functional Service (FSP) solutions.

Join Our Team as an Associate Director Statistical Programming home based in UK Italy or Sweden.

About this role

As part of our Global Biometrics team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals.

TheAssociate Director Statistical Programming is responsible forassisting the Director in leading biometric operations within related departments Statistical Programming.

    Key Responsibilities:

    • Assist the Director in strategic planning leading initiatives and resource allocation for the department. Participate by offering oversight across studies and/or customers including guidance on documentation and output development/review.
    • Assist the Director in proposal development project allocation budget projections and client presentation as needed. Serve as a resource for the department ensuring scientific integrity in the application of statistical methodology to clinical trials.
    • Manage staff in accordance with organizations policies and applicable regulations.
    • Oversees development of direct reports by planning assigning and directing work setting goals appraising performance mentoring and guiding professional development and working with the Director to address any issues.
    • Ensure high quality timeliness and expert review process of the deliverables from the department.
    • Provide advanced technical expertise for internal and external clients. Maintain knowledge and awareness of developments in Biostatistics and clinical trial methodology and regulatory requirements that impact on analyses.
    • Accountable for the project level work of staff including awareness of timelines scope and resourcing strategy. Responsible for guiding leads toward financial success at a study level
    • Provides feedback to draft strategy and initiatives. Implements strategy and initiatives and collects feedback from the implementation (e.g. metrics).
    • Develop and/or provide training to staff across the business unit. Ensures compliance with strategy and initiatives.

    Qualifications:

    • A Bachelor of Science (BSc) or Masters degree in statistics or related discipline; PhD in Statistics or related discipline preferred or equivalent
    • Minimum of 10 years relevant statistical experience in pharmaceutical or CRO industry with increasing levels of responsibility
    • Familiarity with most complex statistical methods that apply to Phase IIV clinical trials.
    • Indepth knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
    • Strong working knowledge of SAS CDISC and Regulatory Submissions.
    • Experience in project management problemsolving and team leadership
    • Ability to deal effectively with sponsors and internal customers at all levels
    • Willingness and ability to travel on occasion
    • Excellent verbal and written communication skills in English

      What We Offer

      We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients

      A Bit More About Us

      Our journey began over 27 years ago in Sweden in the city of Lund. As a fullservice global Contract Research Organization (CRO) we build solutiondriven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.

      Our core values of Trust Quality Passion Flexibility and Sustainability are our guiding light serving as the framework for decisionmaking at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

      Employment Type

      Full Time

      Company Industry

      About Company

      Report This Job
      Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.