Job Description

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Work Schedule

Second Shift (Afternoons)

Environmental Conditions

Office

Job Description

Senior Manager, BiostatisticsJob Description

  • Manages a team within the department who are responsible for the statistical aspects of clinical trials from design through analysis and reporting including client or regulatory interactions.
  • Able to act as the lead statistician, project lead, senior reviewer or project oversight on select projects.
  • Contributes to study proposals and bids representing the department at bid defenses.
  • Organizes teams and implements strategies to ensure smooth operation and project financial success.
  • Coaches staff to provide effective oversight for strategic client relationships and/or oversight for significant client portfolios.
  • Manages staff which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, behavioral and technical coaching and mentoring, employee counseling and separations.
  • Approves courses of action on salary administration, hiring, corrective action and terminations.
  • Reviews and approves time records, expense reports, requests for leave and overtime.
  • Promotes all aspects of PPD Equal Employment Opportunity policy and Affirmative Action Plan.
  • Assures department adherence to good scientific, ethical and regulatory standards.
  • Ensures the effective resource and utilization management of staff.
  • May act as lead statistician, project lead, senior reviewer or project oversight on multiple projects, manages project team resources, budget, finance, timelines and ensures SOP compliance with appropriate documentation.
  • May serve as the randomization statistician on selected projects.
  • Produces sample size calculations.
  • Provides input into study design and statistical considerations during protocol development.
  • Reviews protocols for completeness, appropriateness of clinical design and sound statistical analysis.
  • Contributes to writing appropriate protocol sections.
  • Supports and coaches staff to prepare and review statistical reports, clinical study reports, integrated summaries of safety, integrated summaries of efficacy and other documents as required.
  • Contributes statistical methods section for integrated clinical statistical reports.
  • Reviews integrated clinical statistical reports.
  • Coaches staff to effectively communicate with sponsors concerning project work scope and budgetary changes after reviewing with management.
  • Aids departmental management in process improvement strategies.
  • Suggests, assesses and provides leadership in the department for such initiatives.
  • Conducts training and implementation of new procedures and new industry knowledge.
  • Supports strategic client franchise leadership.

Qualifications

  • Masters degree in statistics, biostatistics, mathematics or related field with 7 years experience preferring at least 8 years of clinical trial experience as a statistician.
  • Previous experience that provides the knowledge, skills and abilities to perform the job.
  • 2 yrs of management responsibility.
  • Demonstrated initiative and motivation.
  • Capable of leading complex projects.
  • Effective management skills as shown through the successful management of multiple projects and staff members and proven ability to mentor and motivate staff.
  • Strong verbal and written communication skills including proficiency in the English language.
  • Positive attitude and the ability to proactively direct and promote teamwork in a multidisciplinary team setting.
  • In-depth knowledge of SAS and clinical biostatistics.
  • In-depth understanding of the drug development process and FDA regulations.
  • Capable of managing change and uncertainty to optimize positive outcomes.

Additional Responsibilities

  • Interprets and administers policies, processes and procedures that may affect sections and subordinate work units.
  • Acts as advisor to subordinates to meet schedules and/or resolve technical problems.
  • Requires full knowledge of own area of functional responsibility.
  • Manager role with significantly larger management scope e.g. global or regional responsibilities or multiple departments OR mastery of manager skills and responsibilities as demonstrated by consistent multi-year successful performance.
  • In some instances may be responsible for a functional area as determined by executive management and not have subordinate supervisors or employees.
  • Assignments are defined in terms of activities and objectives.
  • Work is reviewed upon completion for meeting timelines, adequacy and objectives.
  • Interacts frequently with internal personnel and outside representatives at various levels.
  • Participates and may present at meetings with internal and external representatives.
  • Interaction typically concerns resolution of operational and scheduling issues concerning projects and/or contractual clarifications.

Work Environment

  • Work is performed in an office environment with exposure to electrical office equipment.
  • Domestic travel required occasionally, international travel required rarely and will be determined by client/department needs.
  • Constant interactions with associates and clients required.
  • Exposure to high pressure deadlines.
  • Intense concentration required.
  • When necessary, work additional hours to meet timelines.
  • Exposure to and use of electrical equipment required constantly.
  • Frequently stationary for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands and wrists.
  • Occasional mobility required.
  • Occasional crouching, stooping, bending and twisting of upper body and neck.
  • Light to moderate lifting and carrying or otherwise moves objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Ability to communicate moderately complex information and ideas so others will understand with the ability to listen to and understand information and ideas presented through spoken words and sentences.
  • Frequently interacts with others, relates sensitive information to diverse groups.
  • Ability to apply basic principles to solve conceptual issues.
  • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence.
  • Ability to perform under stress.
  • Ability to multitask.
  • Regular and consistent attendance.

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Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: Philippines City: Manila
Company Website: http://mygwork.com/ Job Function: Clinical & Lab Research
Company Industry/
Sector:
Financial Services

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