Associate Manager, Statistical Programming
4 weeks ago
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Job Responsibility
Monitors staff projects quality, timelines and budgets to foresee and correct issues and assure project expectations are met.
Help staff identify resource or scope of work changes.
Effectively communicate the status of projects to line management and project managers
Work closely with leads to ensure that staff resources are used efficiently, and team is well utilized
Manages resources within team: new hires, terminations, transfers, and contractors
Carry out line management responsibilities for assigned staff, including Performance Management and Development activities, disciplinary procedures and administrative activities
Helps encourage staff career growth and development
Provides statistical programming support and technical support to team members
Act as the lead programmer overseeing technical planning for increasingly complex projects including global and multiple study projects, ISS and ISE, and electronic submissions
Contribute to ongoing improvement of programming processes, methodology and documentation
Keeps abreast of new statistical programming practices, methods and tools, regulatory practices, and industry trends to stimulate departmental growth.
Qualifications (Minimum Required):
Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
Experience (Minimum Required):
Min 8 years of experience, or an equivalent combination of education or experience to successfully perform the key responsibilities of the job.
Extensive experience and proven skills in the use of SAS® programs within a clinical trials environment including all processes/practices used with a Statistical Programming environment.
Knowledge in all aspects of clinical trials from initial study set-up to study completion with an excellent understanding of the roles and responsibilities of all related disciplines, e.g., Biostatistics and Clinical Data Management.
Strong supervisory skills, and ability to organize their own and others' work.
Good problem-solving skills, and a willingness to take ownership of decision-making.
Interpersonal and effective communication skills; able to communicate appropriately throughout Fortrea and with its clients.
Knowledge of the metrics, tools and processes used to manage projects
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
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