Future Talent Program - Clinical and Regulatory Strategic Communications - Intern

Company: 1000 Merck Sharp & Dohme LLC Title: 2027 Future Talent Program - Clinical and Regulatory Strategic Communications - Intern Location: USA - New Jersey - Rahway, USA - Pennsylvania - North Wales (Upper Gwynedd) Posted Date: Posted Today Employment Type: Full time Sidebar Info: Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Job Description: Job DescriptionThe 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 companyThe drug development processDocuments needed to conduct clinical trials and gain approval for new medicinesInformed consentDisclosure of clinical trial information to the publicHealth literacy and plain language conceptsQuality, compliance, operational excellence, that support clinical research executionClinical 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.Required Education and Skills: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 programIs available to work full-time for 12 consecutive weeks beginning in June of 2027Possesses strong Microsoft Office skillsDemonstrates strong scientific communication skills, including the ability to write scientific documents (e.g., lab reports, publications, dissertations, theses, abstracts) and deliver scientific presentationsPreferred Experience and Skills:Motivation to explore a career in medical writingExperience using artificial intelligence tools, especially those that use large language modelsDemonstrated critical thinking and problem-solving capabilitiesExperience collaborating with others on project teamsTime 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.Please note that this position may be closed before the posted end date or may remain open longer, at the discretion of the company. Salary range:The salary range for this role is $39,908 - $111,111 USD.FTP2027RL2027Required Skills:Preferred Skills:Current Employees apply HERECurrent Contingent Workers apply HEREUS and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your RightsEEOC GINA SupplementWe 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 ActsSan Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance OrdinanceLos 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 OrdinanceSearch 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. Employee Status: Intern/Co-op (Fixed Term)Relocation:No relocationVISA Sponsorship:NoTravel Requirements:No Travel RequiredFlexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:10/9/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.