TenaflyRecruiter Since 2001
the smart solution for Tenafly jobs

Senior Manager, Clinical Data Solutions

Company: Takeda Pharmaceutical
Location: Hillsdale
Posted on: November 22, 2021

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 DescriptionREMOTE OPPORTUNITYSenior Manager, Clinical Data SolutionsAs the Senior Manager Clinical Data Solutions, you will oversees and high-quality data management deliverables supporting the Takeda portfolio. You will report to the Director, Clinical Data Solutions of Neuroscience. You will conduct oversight of Data Management activities at the program level - as performed by Strategic Partners, CROs or other 3rd Party Vendors - to ensure they meet obligations as described in ICH-GCP and Takeda's Scope of Work, maximize effectiveness and maintain budgets.You will be an expert for clinical data management, whether directly or by way of mentoring other [junior] CDS Staff. You will lead team members to perform proper Data Reviews, and provide guidance on CDISC standards.Key AccountabilitiesOversee vendor oversight activities across global development programs. Represent data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and Takeda for all data related deliverables, especially to support essential decisions and regulatory submissions.Contribute influential leadership in collaboration with other Takeda Partners to ensure established deliverables are met with the highest degree of quality.Partner with appropriate team members and CRO partners to avoid and resolve risks.Provide input to functional governance with Takeda's strategic suppliers. Partner with appropriate team members to resolves issues escalated from the vendor and teams.Participate in preparing function for submission readiness and may represent function in a formal inspection or audit.Represent function in formal inspections and audits.Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.Ensure achievement of major data management deliverables with other departments including the Therapeutic Area Units, Clinical Operations, Statistical Programming and Statistics.Manage external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting.Be a process expert for operational and oversight models.Maintain SOPs, process maps and templates and timelines to support operational and oversight models.May prepare metrics to support the function's Goals.Represent function in external professional plans and organizations such as SCDM, CDISC, DIA to identify industry best practice and increase the visibility of Takeda.Contribute and lead functional Continuous Improvement plans, providing strategic direction and identifying important deliverables that meet timelines, budget, and are with company, departmental requirements.Ensure compliance with own Learning Curricula, corporate and GXP requirements.Work to ensure the quality of the data in each database delivery, and quality of other data management deliverablesEducational QualificationsBS/BA required preferably in a health-related, life science area or technology-related fields.Experience8 years data management and drug development process with expertise in the interfaces with the data management function.Experience with project management managing data management activities for large drug development programs.Experience with all phases of development in one or more therapeutic areas.NDA/CTD Experience preferred.Knowledge of data management best practices & technologies as applied to clinical trials.Experience with clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes.Expert knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process.Expert in Phase II/Late Phase Neuro studies preferred.Special SkillsExperience with budget planning & management.Knowledge of relational databases and experience using multiple clinical data management systems.Knowledge of general medical coding in the pharmaceutical/biotechnology industry including knowledge of medical dictionaries, coding tools, and coding governance models.Expert knowledge of CDISC standards, SDTM preferred. Good experience leading standards selection and implementing in clinical trials is ideal.Expert knowledge of general of medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processes.Travel RequirementsDomestic/international travel (5-20%) to other Takeda sites, strategic partners, and therapeutic area events may be required.Location: Cambridge - VirtualBase Salary Range: $150,000-170,000 based on candidate professional experience level. Employee may also be eligible for Short Term and Long Term incentive benefits. Employees are eligible to participate in Medical, Dental. Vision, Life Insurance, 401(k), Charitable Contribution Match, Company Holidays, Personal & Vacation Days, Student Loan Repayment Program and Paid Volunteer Time Off. If candidate is not eligible for any benefits or other comp., those can be excludedThis posting is made in compliance with Colorado's Equal Pay for Equal Work Act, C.R.S. -- - 8-5-101 et seqAbsent an approved religious or medical reason, all US office-based and lab-based Takeda employees who work fully on-site or in a hybrid model (as determined by Takeda) must be fully vaccinated to work at a Takeda site or to engage with Takeda colleagues or anyone else on behalf of Takeda. US field-based employees must be fully vaccinated as a condition of employment, absent an approved religious or medical reason. US employees who work at a Takeda manufacturing facility, and those who work at a BioLife center or BioLife lab, may be subject to different guidelines. If you are contacted by a Takeda recruiter about your job application, we encourage you to seek more information on the applicable guidelines for the Business Unit/Function to which you have applied.EEO StatementTakeda 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.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Keywords: Takeda Pharmaceutical, Tenafly , Senior Manager, Clinical Data Solutions, Executive , Hillsdale, New Jersey

Click here to apply!

Didn't find what you're looking for? Search again!

I'm looking for
in category

Log In or Create An Account

Get the latest New Jersey jobs by following @recnetNJ on Twitter!

Tenafly RSS job feeds