drjobs Senior Specialist, Scientific Reference Data

Senior Specialist, Scientific Reference Data

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1 Vacancy
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Job Location drjobs

Rahway, NJ - USA

Monthly Salary drjobs

$ 114700 - 180500

Vacancy

1 Vacancy

Job Description

Job Description

Be part of a dynamic team that is dedicated to accelerating research and innovation. We are seeking a passionate Senior Specialist to join our Scientific Reference Data this position you will be responsible for delivering and maintaining standardized reference data utilized across the company to promote a frictionless exchange of scientific cross-divisional data. A successful Senior Specialist will be open to explore and leverage multiple tools internal and external reference databases and automation solutions in the pursuit of providing accurate consistent and timely shared reference data. The ideal candidate will possess scientific acumen along with strong data handling technical skills a penchant for accuracy and consistency excellent communication skills and a background in pharma/biotech. Previous experience with implementing and managing clinical and regulatory data standards is a big plus. If you believe in the power of a strong data foundation as an accelerator of scientific progress and are committed to ensuring excellence in data standardization we invite you to apply to our team.

Primary activities include but are not limited to:

  • Identifying evaluating & implementing new scientific clinical and regulatory reference data sources

  • Ensuring timely authoring publication and maintenance of reference data in a centralized database

  • Defining data quality rules for reference and master data

  • Defining data stewardship workflows and access policies

  • Utilizing knowledge of the drug development process and of master data principles to assign company identifiers and descriptive metadata for small molecules biologics vaccines & medical devices

  • Creating and maintaining documentation operating procedures and training materials to enable adherence to relevant standards and policies

  • Performing regular data integrity reviews and technical analysis in addressing data quality issues

  • Contributing as a key player in defining and enabling reference data ingestion and maintenance processes

  • Maintaining current knowledge of industry data standards for pharmaceutical products and associated activities

  • Supporting maintenance and SDLC testing for reference data systems

  • Building and maintaining excellent relationships with IT partners end users/stakeholders including active outreach and engagement

  • Identifying opportunities to improve efficiency effectiveness and quality and implement changes

Education Requirements:

  • Degree in life sciences information science or related scientific discipline plus pharma/biotech industry or healthcare experience

    • Bachelors and 5 years experience

    • Masters/PhD and 3 years experience

Required Experience and Skills:

  • Familiarity with ontologies data standards taxonomies and terminologies relevant to the biomedical industry (e.g. ICH MedDRA CDISC HL7 EMA SPOR GSRS IDMP WHO-Drug and ATC classes Snomed MeSH)

  • Experience with reference data management systems content and processes

  • Experience in master data management data standards and business rules provenance and stewardship

  • Experience with data modeling automation and scripting tools to manage extract manipulate and report data

  • Experience or understanding of drug discovery development and research clinical data coding and experience working within a regulated environment

  • Ability to engage stakeholders to determine reference/master data requirements in support of their business needs and deliver the data solution

  • Excellent written and verbal communication skills with the ability to convey technical and business information

  • Strong prioritization and project management skills with high attention to detail

  • Ability to work with minimal oversight within a matrixed environment to drive tasks to completion and to act with appropriate accountability

  • Excellent customer service orientation with prompt response to inquiries

  • Ability to work under pressure in a changing environment with flexibility

  • Proficiency with collaboration and productivity tools (MS Teams Jira Confluence Excel MS Power Automate etc.)

Preferred Experience and Skills:

  • Experience in designing and developing custom reference data controlled vocabularies taxonomies ontologies

  • Familiarity with the implementation of FAIR principles

  • Experience with data structures (e.g. relational hierarchical graph) and data exchange formats (e.g. JSON XML RDF)

  • Experience with data engineering tools (i.e. SQL Python Power Automate etc.)

  • Experience with cloud-based data platforms and APIs for extracting processing and sharing reference data

  • Knowledge of text mining machine learning and natural language processing for data curation and enrichment

  • Familiarity with small molecules biologics vaccines and medical devices

  • Experience with biomedical and/or chemical searching resources (SciFinder STN Medline/PubMed Dialog etc.)

  • Experience writing and maintaining process documentation

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race color age religion sex sexual orientation gender identity national origin protected veteran status disability status or other applicable legally protected a federal contractor we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences perspectives skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas broad experiences backgrounds and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anothers thinking and approach problems collectively.

Learn more about your rights including under California Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5 2023 employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week Monday - Thursday although the specific days may vary by site or organization with Friday designated as a remote-working day unless business critical tasks require an on-site Hybrid work model does not apply to and daily in-person attendance is required for field-based positions; facility-based manufacturing-based or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note this Hybrid work model guidance also does not apply to roles that have been designated as remote.

The salary range for this role is

$114700.00 - $180500.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive if applicable.

We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of applicable state and local laws including the City of Los Angeles Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Adaptability API Platforms Automation Biopharmaceuticals Biopharmaceutics Change Management Data Analysis Data Curation Data Engineering Data Integrity Data Management Data Quality Data Requirements Data Standards Data Stewardship Data Taxonomy Good Manufacturing Practices (GMP) Key Performance Indicators (KPI) Master Data Management (MDM) Project Management Project Prioritization Reference Data Reference Data Management Taxonomy Management

Preferred Skills:

API Development Business Process Automation Clinical Data Interchange Standards Consortium (CDISC) Standards Drug Development Drug Discovery Process ICH Guidelines ISO IDMP MedDRA Microsoft Power Automate Ontology Development Resource Description Framework (RDF) Script Development SNOMED CT Structured Query Language (SQL) Writing Technical Documents

Job Posting End Date:

09/5/2025

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Senior IC

Employment Type

Full-Time

About Company

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