Clinical Data Analyst

Company: Takeda Pharmaceutical
Location: Newark
Posted on: March 16, 2023

Job Description:

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.Join Takeda as a Senior Manager, Programming where you will work with Clinical Data Standards and Clinical Data Management teams in the development of data cleaning/quality checks, study status metric, and monitoring reports standards.--You will also lead and organize programming activities for assigned clinical studies and projects--As part of the Submission Excellence Programming team you will report to the Director or Senior Director, Programming and work with other analysts, Clinical Data Managers, and other roles as needed to apply standards and--develop data cleaning reports to support of the data review plan.How you will contribute: Create data cleaning reporting solutions with appropriate oversight that support the quality and timely delivery of data cleaning, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans.--Create any needed documentation for reports throughout the lifespan of the study and/or asset for all deliverables--Complies with applicable SOPs and work practices--Serves as a technical resource to the study teams for data visualization and reporting tools--Supports knowledge development of others on reporting tools that support the accuracy and integrity of study data--Provide programming expertise for data cleaning to efficiently ensure high quality data--Enhances available reporting tools/macros or creates new ones to support the review of clinical trial data and trial status information for cross-functional use and provides input on data management reporting standards as required--Ensure accurate delivery by creating macros for Standard listings for the department based on specifications.--Creates and tests listings for data review.--Develop programs that generate CRF and Query metrics, including ad-hoc Sponsor and internal programming requests.--Ensures operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan, in collaboration with the Clinical Data Management--Directly supports knowledge development of others on data reporting and reporting tools that support the accuracy and integrity of study data--Identifies existing process/product improvements--Develops innovative, advanced new concepts that improve processes----Recognizes development needs and identifies/creates development opportunities within team--Supports the development of the Data Management Programming talent base and identifies development needs within the area of responsibility--Minimum Requirements/Qualifications: MS with -6+ years of industry related experience.----BS with -8+ years of industry related experience.--Proven track record of contributing to business process transformation and organizational culture change as well as providing programming expertise on programs with complex business deliverables--Experience leading business process transformations and organizational culture change as well as contributing to programming expertise on programs with complex business deliverables--Operational experience in pharmaceutical drug development with significant direct exposure to clinical development and data operations required for the reporting of clinical trial data (e.g. data review, regulatory submissions, safety updates, etc.)--Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable--Strong communication (written and oral), leadership, decision-making, influencing, negotiation, and project management skills--Demonstrated experience managing complex projects and developing successful partnerships within and across functional areas--Technical skills and experience using relational databases (e.g. MS SQL Server, Redshift, or Oracle), SAS and data visualization tools (e.g. BOXI, Spotfire, Tableau, RShiny, JReview)--EDC build and/or clinical data management experience preferred--Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)--Programming, specifically SAS and R, and other visualization tools hands-on experienceWhat Takeda can offer you: Comprehensive Healthcare: Medical, Dental, and VisionFinancial Planning & Stability: 401(k) with company match and Annual Retirement Contribution PlanHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach Programs and company match of charitable contributionsFamily Planning SupportFlexible Work PathsTuition reimbursementMore about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.Base Salary Range: $124,600 $178,000, based on candidate professional experience level.-- Employees may also be eligible for Short Term and Long-Term Incentive benefits as well. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time OffThe final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience.In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.Empowering our people to shine: Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations Boston, MA Worker Type Employee Worker Sub-Type RegularTime Type Full time

Keywords: Takeda Pharmaceutical, Newark , Clinical Data Analyst, Professions , Newark, New Jersey