Data Science

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research Labs Division can provide you with great development and a chance to see if we are the right company for your long-term goals., Seeking a highly motivated individual who is pursuing an education in the life sciences, medicine, pharmacology/pharmacy, quality, operations, data science, or a related field, and who is interested in writing, communicating about medicine and science, and supporting the quality, compliance and operational excellence activities that enable clinical research. The goal of this position is for the individual to gain broad insight into the following:

• The roles of several types of medical writers at a large pharmaceutical company
• The drug development process
• Documents needed to conduct clinical trials and gain approval for new medicines
• Informed consent
• Disclosure of clinical trial information to the public
• Health literacy and plain language concepts
• Quality, compliance, operational excellence, that support clinical research execution

Clinical Regulatory & Strategic Communications (CRSC) is a multidisciplinary organization that plays a critical role in supporting the development of new medicines by creating key clinical and regulatory documents, communicating clinical trial results, and ensuring information is shared responsibly and transparently with regulatory agencies, healthcare professionals, trial participants, and the public.

The department develops and manages essential clinical trial documents, including study protocols, informed consent forms, investigator brochures, clinical study reports, and regulatory summaries. CRSC also supports public disclosure activities by creating technical and plain-language summaries of clinical trial information and results. We also drive quality, compliance, continuous improvement, and adoption of innovative technologies, including artificial intelligence, to enhance the efficiency and effectiveness of CRSC operations.

The Summer Intern will participate in a variety of projects and learning experiences that provide exposure to how clinical trials are designed, conducted, reported, disclosed, and supported through quality and operational excellence practices. Working under the guidance of a mentor, the intern will gain both hands-on and observational experience while collaborating with individuals and teams across the organization., Research Brochures Operations Management Innovation Data Science Communication Data Analysis Life Sciences Technology Use Pharmaceuticals Self-Motivation Clinical Trials Problem Solving Business Process Microsoft Office Drug Development Informed Consent Telephone Skills Project Delivery Clinical Research Critical Thinking Laboratory Reports Process Improvement Regulatory Documents Contingent Workforce Overcoming Obstacles Science Communication Operational Excellence Clinical Study Reports Artificial Intelligence Strategic Communication Continuous Improvement Process +0 2027 Future Talent Program - Clinical and Regulatory Strategic Communications - Intern Merck & Co., Inc

Rahway, NJ*On-Site

Writing Research Brochures Operations Management Innovation Data Science Communication Data Analysis Life Sciences Technology Use

Data Analysis Life Sciences Technology Use Pharmaceuticals Self-Motivation Clinical Trials Problem Solving Business Process Microsoft Office Drug Development Informed Consent Telephone Skills Project Delivery Clinical Research Critical Thinking Laboratory Reports Process Improvement Regulatory Documents Contingent Workforce Overcoming Obstacles Science Communication Operational Excellence Clinical Study Reports Artificial Intelligence Strategic Communication Continuous Improvement Process, * Has completed at least 3 years of a bachelor’s or equivalent program in a scientific discipline (e.g., life sciences, data science, pharmacy, or medicine) and be currently enrolled in a degree program

• Is available to work full-time for 12 consecutive weeks beginning in June of 2027
• Possesses strong Microsoft Office skills
• Demonstrates strong scientific communication skills, including the ability to write scientific documents (e.g., lab reports, publications, dissertations, theses, abstracts) and deliver scientific presentations

Preferred Experience and Skills:

• Motivation to explore a career in medical writing
• Experience using artificial intelligence tools, especially those that use large language models
• Demonstrated critical thinking and problem-solving capabilities
• Experience collaborating with others on project teams
• Time management skills (e.g. manages multiple projects/assignments & delivers each on time and with high quality, overcomes obstacles that impact project delivery)
• Interest in quality, compliance, operational excellence, data analysis, process improvement, or practical technology use to improve business processes., Self-Motivation Clinical Trials Problem Solving Business Process Microsoft Office Drug Development Informed Consent Telephone Skills Project Delivery Clinical Research Critical Thinking Laboratory Reports Process Improvement Regulatory Documents Contingent Workforce Overcoming Obstacles Science Communication Operational Excellence Clinical Study Reports Artificial Intelligence Strategic Communication Continuous Improvement Process

The salary range for this role is $39,908 - $111,111 USD.

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully 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.