Senior Associate, Senior Data Manager

United States - Pennsylvania - CollegevilleUnited States - New York - New York CityPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Our mission is simple : empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will Achieve Support healthcare decisions that ensure the safe and effective use of medications. Your role is vital in developing frameworks to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, and exploring ways to bridge data gaps. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.How You Will Achieve It Contribute to moderately complex projects, managing time effectively to meet targets and develop short-term work plans.Take on the role of Data Manager for clinical trials, overseeing Data Monitoring and Management (DMM) activities.Collaborate with partners and colleagues to ensure operational excellence and apply standards while developing data cleaning reports.Maintain high standards across all DMM deliverables and ensure data quality and completeness as specified in the Data Management Plan.Document and share lessons learned during studies to promote cross-study learning.Build strong relationships with local and global subject matter experts (SMEs) to leverage their expertise in systems and processes, proactively identifying issues and developing solutions.Qualifications Must-Have BA / BS with at least 2 years of experience or MBA / MS with any years of experienceDemonstrated knowledge of data management processes and principlesProficiency in web-based data management systemsWorking knowledge of electronic document management systemsFamiliarity with the International Conference on Harmonization, particularly Good Clinical PracticesThorough understanding of clinical study management and regulatory operations processesEffective verbal and written communication skillsNice-to-Have Relevant pharmaceutical industry experienceExperience using data visualization toolsProficient experience using commercial clinical data management systems and / or EDC productsAwareness of regulatory requirements and relevant data standardsStrong analytical and problem-solving skillsAbility to work collaboratively in a team environmentExcellent organizational and time management skillsOther Job Details : Last Date to Apply for Job : 2 28 JANUARY 2025Eligible for Employee Referral BonusNot Eligible for Relocation AssistanceWork Location Assignment : HybridThe annual base salary for this position ranges from $80,300.00 to $133,900.00. This position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive benefits to help our colleagues lead healthy lives and support each of life’s moments, including a 401(k) plan with Pfizer Matching Contributions, paid vacation, holiday and personal days, paid caregiver / parental and medical leave, and health benefits including medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits.Why Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Our mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.EEO & Employment EligibilityPfizer is committed to equal opportunity in employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment. This position requires permanent work authorization in the United States.#J-18808-Ljbffr

Salary : $80,300 - $133,900