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Merck Global Clinical Data Standards, Vocabulary Specialist in Austin, Texas

Job Description

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.

The Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a subject matter expert in CDISC Controlled Terminology and applying terminology and associated reference data to data collection and transformation specifications in compliance with Health Authority regulations and guidance and company best practices.

The Vocabulary Specialist is able to:

  • Work independently, collaboratively as a member of a team, or successfully as a leader, with equal effectiveness.

  • Interact with staff across multiple of our company's sites.

  • Promote teamwork across GCDS by actively communicating and proactively sharing information

  • Support senior/leadership roles, in areas of observed competence, to enhance standards and associated processes for growth opportunities

The Vocabulary Specialist may lead or participate in:

  • Internal clinical data standards forums

  • Standards development teams and data governance reviews

  • Strategic and process improvement/design projects

  • Industry forums and standards development teams

  • The Vocabulary Specialist maintains knowledge of new technologies, clinical study data standards, regulatory requirements emerging in industry, and our company's guidelines and SOPs.

Required Experience:

  • 5+ years of work experience in pre-clinical and/or clinical research to include minimum 2 years’ experience in data standards, with a strong emphasis on managing and applying Clinical Data Interchange Standards Consortium (CDISC) Controlled Terminology.

Preferred Experience:

  • C DISC Standards and the application of SDTM and its associated controlled terminology.

  • Knowledge of clinical research-controlled terminology (i.e., MedDRA, WHODD, SNOMED).

  • Understanding of a variety of external data types (i.e., genetics, immunogenicity, PK/PD).

  • Understanding of collection and terminology associated with questionnaires.

  • Understanding of lab values and the importance and maintenance of unit of measure conversions.

  • Knowledge of versioning and maintenance of controlled terminology.

  • Excellent communication/presentation skills.

  • Must have an innovative spirit, outstanding interpersonal skills, leadership and demonstrated proficiency in the management of multiple projects.

Education:

  • B.A. or B.S. degree, preferably in life sciences (i.e., Medical Technology, Medical Laboratory Scientist, Clinical Laboratory Scientist, Nursing), or equivalent experience in relevant discipline.

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If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separationpackage, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.

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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, generally Tuesday, Wednesday and either Monday or 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 presence. This 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”.

Under New York State, Colorado State, Washington State, and California State law, the Company is required to provide a reasonable estimate of the salary range for this job. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.

Expected salary range:

$135,500.00 - $213,400.00

Available benefits include bonus eligibility, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. For Washington State Jobs, a summary of benefits is listed here (https://www.benefitsatmerck.com/) .

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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:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

No

Requisition ID: R287488

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