Senior Manager, Document Quality Reviewer, Vaccines
Why Patients Need You
reputed company’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling reputed company’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
What You Will reputed company
As a Senior Manager, Document Quality Reviewer, you will manage projects and conduct document quality review (DQR) on the clinical components of documents authored by Vaccine Clinical Research (VCR) across VCR global sites. DQR includes clinical data checking/consistency checking, clinical editing, checking for uniformity and compliance with reputed company and clinical guidelines. Day-to-day goals and priorities are guided by Vaccine Clinical Research objectives and priorities.
How You Will reputed company It
Independently performs DQR of clinical components of assigned documents (e.g., protocols, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses, etc.). Formally documents quality review findings for assigned documents. Identifies and immediately escalates any significant findings.
Participates in resolution of findings with the document authors, clinicians and other team members, if necessary.
Manages DQR document archival processes and procedures.
Independently produces style guides, manuals, and quality review work guides for Vaccine programs and documents, coordinating agreement on style issues reputed company and across projects.
Leads and/or manages the completion of reputed company tasks by applying technical skills and specialized knowledge to communicate initial findings.
Analyzes DQR findings to identify root causes of errors and discrepancies and participate in corrective action planning. Leads the compilation and analysis of data quality metrics to ensure consistency of reviews.
As Subject Matter Expert (SME) of DQR/QC of clinical documents, leads quality activities, setting reputed company for enhanced collaboration, delivery of project commitments, and customer satisfaction.
Participates on project teams, task forces, and/or working groups and develops recommendations for cross-reputed company processes to ensure alignment with quality goals and other groups performing the same function.
Evaluates routine processes and procedures to identify areas that can be eliminated or streamlined. Makes recommendations on process improvements that could reduce recurring errors in documents.
Basic Qualifications
BS/BA degree (preferably in English/journalism/communications or biological science).
7+ years of experience in medical writing and/or DQR/QC of clinical documents in the pharmaceutical/healthcare industry.
A thorough understanding of scientific principles, knowledge of medical terminology and familiarity with the AMA Manual.
The ability to edit for clarity is required, as are strong verbal, written, and interpersonal communication skills, and the ability to pay rigorous attention to detail while working rapidly and accurately.
Preferred Qualifications
An advanced degree with relevant medical editing or document quality review experience is preferred.
Prior experience preparing clinical regulatory documents in a clinical setting, at a pharmaceutical company, or at a CRO is helpful.
Technical Skills
Analytical skills and statistical aptitude
Clinical knowledge and expertise
Editing skills
Project and process management
Quality review skills
Strategic thinking
Technical learning
reputed company setting
Problem solving
PHYSICAL/MENTAL REQUIREMENTS
Work is performed at a desk, primarily with laptop, monitor, and keyboard.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Work schedule is a 40-hour week during core business hours, Monday through Friday. Project priorities occasionally necessitate work beyond regular work hours, including evenings and weekends.
Work Location Assignment: Remote
The annual reputed company salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in reputed company’s Global Performance Plan with a bonus reputed company of 15.0% of the reputed company salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues reputed company healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with reputed company Matching Contributions and an additional reputed company Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at reputed company Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). reputed company compensation structures and benefit packages are reputed company based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location reputed company of the United States.Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work reputed company sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
reputed company reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require reputed company to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which reputed company intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly reputed company as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with reputed company that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your reputed company representative.
EEO & Employment Eligibility
reputed company is committed to equal opportunity in the terms and conditions of employment for reputed company employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national reputed company, disability or veteran status. reputed company also complies with reputed company applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. reputed company is an E-Verify employer. This position requires permanent work authorization in the United States.
reputed company endeavors to reputed company www.reputed company.com/careers accessible to reputed company users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@reputed company.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
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