Associate Director - Global Data Operations

<p style="text-align:left">Job Description</p><p style="text-align:inherit"></p><p>Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards.</p><p></p><p>Under the direction of the GDO (Global Data Operations) leadership, the GDO Operations Manager is responsible for leading Senior clinical data managers (SCDMs) and Clinical Data Managers (CDMs) in operations tasks, both strategic and tactical in nature, within a Data Management Center (DMC). They are responsible for ensuring the consistent execution of quality processes and deliverables and managing the workload and development of their direct staff. Encourages effective interaction of DMC staff with business partners to achieve common objectives.</p><p></p><p><b><i>Primary activities include, but are not limited to:</i></b></p><ul><li><p>Direct Line Management of SCDM and CDMs</p></li><li><p>Escalates to appropriate leadership/management as needed as risks and needs arise in the business</p></li><li><p>Increases functional effectiveness by supporting departmental efforts to simplify and standardize procedures to the greatest extent possible</p></li><li><p>sharing best practices and participating or leading in continuous improvement efforts.</p></li><li><p>Participates in or Leads GDO Business Excellence Networks (BENs), GDO improvement efforts, SME networks, GDO and/or GDMS special initiatives as needed</p></li><li><p>Facilitates and/or participates in management and functional area meetings, contributing expertise, when necessary, through formal or informal presentations.</p></li><li><p>Keeps abreast of process and technology changes both within and outside of our company that may impact staff.</p></li><li><p>May support any other projects or perform any other data management task deemed appropriate by management.</p></li><li><p>Supports GDO management team to set objectives and lead the team to achieve the business goals.</p></li><li><p>Leads and/or participates in initiatives beyond GDO or GDMS (e.g., cross-divisional projects, cross-industry initiatives, etc.).</p></li><li><p>Trains staff on business processes, operations and tools</p></li></ul><p></p><p><b>Education:</b> B.A. or B.S. degree, preferably in life sciences, computer science, or related discipline.</p><p></p><p><b>Experience:</b> </p><ul><li><p>At least 5 years’ experience in Clinical Trials</p></li><li><p>At least 2 years’ experience in People Management or equivalent demonstrated leadership</p></li><li><p>Minimum one year´ experience in your current role</p></li></ul><p></p><p><b>Knowledge and Skills:</b></p><ul><li><p>Demonstrate ability to build talent and lead teams of 15 or more people, with influencing and development skills.</p></li><li><p>Strong project management, decision making, problem solving, negotiation and communication skills</p></li><li><p>Knowledge and/or experience in Research &amp; Development at Pharmaceutical - Science Research industry.</p></li><li><p>Preferably, knowledge in Databases, Data Analytics</p></li><li><p>Able to work under pressure in a changing environment with flexibility</p></li><li><p>Advance English Level</p></li><li><p>Applying Excel Level</p></li></ul><p></p><p>#OneGDMS</p><p></p><p><b>Required Skills: </b></p>Accountability, Accountability, Adaptability, Business Partnerships, Business Processes, Clinical Data Management, Clinical Trials, Communication, Computer Science, Data Analysis, Data Extraction, Data Integration, Data Validation, Decision Making, Good Clinical Practice (GCP), Interpersonal Relationships, Leadership, Negotiation, People Leadership, People Management, Pharmaceutical Development, Pharmaceutical Research, Pharmacovigilance, PL/SQL (Programming Language), Pressure Management {+ 3 more}<p></p><p><b>Preferred Skills: </b></p><p style="text-align:inherit"></p><p style="text-align:left">Current Employees apply <a target="_blank" href="https://wd5.myworkday.com/msd/d/task/1422$6687.htmld">HERE</a></p><p style="text-align:inherit"></p><p style="text-align:left">Current Contingent Workers apply <a target="_blank" href="https://wd5.myworkday.com/msd/d/task/1422$4020.htmld">HERE</a></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Search Firm Representatives Please Read Carefully </b><br />Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; 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. </p><p style="text-align:inherit"></p><p style="text-align:left"><b>Employee Status: </b></p>Regular<p style="text-align:inherit"></p><p style="text-align:left"><b>Relocation:</b></p>No relocation<p style="text-align:inherit"></p><p style="text-align:left"><b>VISA Sponsorship:</b></p>No<p style="text-align:inherit"></p><p style="text-align:left"><b><span>Travel Requirements:</span></b></p>No Travel Required<p style="text-align:inherit"></p><p style="text-align:left"><b>Flexible Work Arrangements:</b></p>Hybrid<p style="text-align:inherit"></p><p style="text-align:left"><b>Shift:</b></p>Not Indicated<p style="text-align:inherit"></p><p style="text-align:left"><b>Valid Driving License:</b></p>No<p style="text-align:inherit"></p><p style="text-align:left"><b>Hazardous Material(s):</b></p>NA<p style="text-align:inherit"></p><p style="text-align:left"><b>Job Posting End Date:</b></p>04/3/2026<p style="text-align:left"><b><span>*A job posting is effective until 11:59:59PM on the day <u>BEFORE</u> the listed job posting end date. Please ensure you apply to a job posting no later than the day <u>BEFORE</u> the job posting end date. </span></b></p>