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Associate Director, Programming Technology

Laboratory Corporation of America Holdings (Covance)

Durham, North Carolina, United States

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Labcorp Drug Development has an exciting opportunity for an Associate Director, Programming Technology. The Associate Director, Programming Technology can be remotely (home-based) located anywhere within the United States or Canada. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><p style="margin: 1.0pt 0in 1.0pt 0in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong><u>Essential job duties:</u></strong></span></p><ul><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provide leadership at the sub-group level; supporting the Senior Director in Global leadership across Acquisition Configuration, Implementation and Standards (ACIS) function and associated roles within SAIO.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Oversee the development, implementation and adherence to project plans and performance indicators within the clinical operating unit.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provide HR leadership, budget management, administrative and productivity management to ACIS team.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Responsible to liaise with other functional counterparts as necessary to deliver successful projects/programs for the client.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Assist project teams in problem resolution such as deviation from project plans.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ensure project deliverables are met according to both Labcorp Drug Development and client contractual expectations.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provide advanced planning and risk management for programing projects-like issue escalation and resource management.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Own successful achievement of financial and productivity goals in annual budget as it specifically applies to the Acquisition Configuration, Implementation and Standards (ACIS) area.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Interact and collaborate with other project and specialty team members (clinical, programming, statistics, drug safety, data integration, etc.) in order to provide counsel on technical issues impacting their performance and deliverables.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Support the technical mentoring of ACIS and CDM staff in regional locations.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Maintain technical data management competencies via participation in internal and external training seminars.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Review literature and research technologies/procedures for improving global data management practices.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Provide analysis and strategic input on bid proposals, when requested and be the programming leader for all bid-defenses, as required.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ensure no vendor is engaged in any context without connection to IT, Purchasing, and Global EDC Solutions team.</span></li><li style="margin: 1.0pt 0in 1.0pt .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Any other duties assigned by supervisor.</span></li></ul><p style="margin: 0px;"> </p><h2>Education/Qualifications:</h2><p style="margin: 1.0pt 0in 1.0pt 0in;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong><u>Education:</u></strong></span></p><ul><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">University/college degree (life science, computer science, programming, pharmacy or related subject preferred), or certification in a related profession from an appropriately accredited institution (e.g., nursing certification, computer science, medical or laboratory technology). MBA or other Advanced Degree strongly preferred.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Broad knowledge of drug development process.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Financial understanding of global clinical development budgets.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Proven expertise in financial control procedures.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Proven ability to understand and communicate corporate policies.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Thorough knowledge of effective clinical project management and data management practices.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Strong knowledge of resources management systems.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements of the conduct of clinical development programs.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Proven background in performance within complex global management matrix.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Proven background in positive leadership and organizational development in alignment with corporate and business-unit HR strategies.</span></li></ul><p style="margin: 1.0pt 0in 1.0pt 0in;"><span style="font-size: 11.0pt;"> </span></p><h2>Experience:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">IT experience would be preferred.  </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience with System Development Lifecycle (SDLC).  </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience within Pharma, CRO, and/or software organizations.  </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Some knowledge with EDC systems, SAS, and vendor management preferred.  </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">People and technology management will be a must.</span></li></ul><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">#LI-REMOTE</span></p>

Job posted: 2021-09-08

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