Biostatistics, Senior Manager (remote or office) 20K sign-on

Thermo Fisher Scientific Remote
biostatistics senior manager remote team people health leadership lead management oversight senior clinical research
March 25, 2023
Thermo Fisher Scientific
Texas
Are you ready for an amazing opportunity that truly will make a difference, with an amazing team and incredible leadership? If so, you are in the right place! We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD clinical research services thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health (https://www.ppdi.com/about/purpose-mission-strategy) . You will be joining a truly collaborative and winning culture (https://www.ppdi.com/careers/about/culture) as we strive to bend the time and cost curve of delivering life-saving therapies to patients. What will you be doing in this role? Below is more information. Summarized Purpose : 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. Oversees the resourcing of program of studies, or integrated summaries, develops and implements strategies to ensure optimal efficiencies around process, programming and client needs. Provides support, guidance and project leadership to junior and senior team members. Provides oversight for strategic client relationships, and/or oversight for significant client portfolios. Essential Functions : Serves as (or mentors/coordinates staff in the roles of) 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. Serves as (or mentors others in the role of) the randomization statistician on selected projects. Prepares and reviews statistical reports, (or mentors others in the role of) 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. Manages resourcing and delivery strategy of complex books of work - ISS/ISE, submissions etc 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. Participates in strategic client franchise leadership. Provides mentorship and guidance to junior team members; assists people managers with leadership activities, such as interviewing, job description design, etc. Education and Experience : Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years ). Master degree in statistics, biostatistics, mathematics or related field with 8+ years experience In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities : 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 Positive attitude and the ability to proactively direct and promote teamwork in a multi-disciplinary team setting In-depth knowledge of SAS® and clinical biostatistics Strong clinical trial project lead experience that includes managing budgets and timelines Management: No people management responsibilities. EEOC: We are an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary for typical working hours. Ability to use and learn standard office equipment and technology with proficiency. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. May require travel. (Recruiter will provide more details). The salary range estimated for this position is $160,000-185,000. This position will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. Actual compensation will be confirmed in writing at the time of offer. We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally includes: A choice of national medical and dental plans, and a national vision plan A wellness program, and valuable health incentive opportunities for company contributions to a Health Reimbursement Account (HRA) or Health Savings Account (HSA) Tax-advantaged savings and spending accounts and commuter benefits Employee assistance program Paid Time Off, 10 paid holidays annually, 8 hours of volunteer time, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture (https://www.ppdi.com/careers/life-at-ppd) , where PPD clinical research services truly value a work-life balance. We ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel. Our 4i Values: Integrity Innovation Intensity Involvement If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world s most urgent health needs, submit your application we d love to hear from you! *LI-KF1 #PPDHP Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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