Education Minimum Requirement: BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 12-15 years SAS programming experience in a clinical trial environment MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 10 or more years SAS programming experience in a clinical trial environment Required Experience and Skills: Department Required Skills and Experience: - Excellent interpersonal skills and ability to negotiate and collaborate effectively
- Excellent written, oral, and presentation skills
- Superior knowledge and significant experience in setting strategy and developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
- Excellent project management skills; leadership across multiple and complex programs; determines approach and ensures consistency and directs effort others; ability to engage key stakeholders
Position Specific Required Skills and Experience: - Expertise in SAS and clinical trial programming (Safety and Efficacy)
- Superior knowledge and significant experience in setting strategy and developing analysis and reporting statistical programming deliverables (datasets, statistical analyses, report tables, and graphics) using global and TA standards and according to quality, compliance and timeliness requirements
- US and/or worldwide Oncology regulatory application submission experience at the leadership level including the development of electronic submission deliverables
- Designs and develops complex programming algorithms in Oncology area
- Familiarity with statistical analysis methods, terminology and concepts
- Familiarity with clinical data management concepts
- Experience in CDISC ,SDTM and ADaM standards
- Demonstrated success in the assurance of deliverable quality and process compliance
- Strategic thinking - ability to analyze operational activities and challenges and develop and implement strategic solutions
- Ability to anticipate stakeholder requirements
- Ability and interest to work across cultures and geographies
- Ability to manage multiple study deliverables at a time
Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com. Search Firm Representatives Please Read Carefully: Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement |
