Montgomery County Careers – Merck

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merck
Merck, with significant operations in Montgomery County, has entered into a partnership with Seattle Genetics to collaborate on cancer therapies.

Merck, one of the world’s largest pharmaceutical companies, is a global healthcare leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Merck is building a new kind of healthcare company, one that is ready to help create a healthier future for all of us

Associate Director Statistical Programming

This position manages the programmers responsible for statistical programming activities for multiple late stage drug/vaccine clinical development projects. He/she implements departmental objectives and manages resources and operational challenges. The person hires appropriate, qualified staff, manages staff performance and development, including coaching and mentoring, and manages the training plan.

The ideal candidate will possess a bachelor’s degree in an appropriate field plus nine to twelve years of experience in a clinical trial environment, or a master’s degree with a minimum of seven years of experience. He/she will have experience managing a team of statistical programmers in the development and execution of statistical analysis and reporting deliverables in one or more therapeutic areas.

Click here to read more about the Associate Director Statistical Programming position at Merck.

Director, Regulatory Affairs

This position provides expert advice to product development teams and subsidiaries on regulatory issues as they arise throughout the entire life cycle of the drug.  He/she provides leadership to the staff by leading the global regulatory team that coordinates cross-functional regulatory support for development programs and marketed products. The person reviews and provides final approval of local registration study protocols when needed to obtain marketing authorization in secondary markets.

The ideal candidate will possess a bachelor’s degree in an appropriate field with a minimum of 10 years of drug development, clinical experience, or regulatory affairs. Higher degrees with fewer years of relevant experience are also acceptable. He/she will preferably have experience in oncology, immunology, biologics, and regulatory affairs.

Click here to read more about the Director, Regulatory Affairs position at Merck.

Specialist, Digital Publications

This position programs and configures all user-customizable website changes as needed. He/she manages the XML translation site-publishing process to UAT and production servers. The person oversees the evaluation of user test sites by the editorial staff and corrects any structural defects in the XML. He/she works with developers to resolve complex problems.

The ideal candidate will possess a bachelor’s degree. He/she will have three years of experience in computers or information management. The person will have solid understanding and proficiency in HTML, XML, CSS, and JavaScript and in testing methodologies and tools. He/she will have a foundational understanding of databases, SQL, XSL, and graphic design.

Click here to read more about the Specialist, Digital Publications position at Merck.

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