Clinical Operations Educator – Remote

Sep 23, 2025

Merck

Company Website

Biotech, Clinical Research, Nurse Educator, Nurse Practitioner | NP | APRN, Registered Nurse | RN



Employment Type:

Regular | Perm Employee



Schedule:

Full-time

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Remote Status:

Remote with Travel



License:

Any State | US

Merck

Company Website

Biotech, Clinical Research, Nurse Educator, Nurse Practitioner | NP | APRN, Registered Nurse | RN



Employment Type:

Regular | Perm Employee



Schedule:

Full-time



Remote Status:

Remote with Travel



License:

Any State | US

Job DescriptionWe are seeking three experienced and highly motivated individuals to join our team for a Clinical Operations Educator position. As Clinical Operations Educator you will be fully dedicated to training and education activities supporting the monitoring roles in clinical operations e.g. Clinical Research Associate (CRAs), Clinical Research Managers (CRMs), in the Global Clinical Trial Operations (GCTO) Regions in alignment with strategic priorities for the Regions, supporting an organization of more than 4000 FTEs. This role focuses on creating role-based, therapeutic area-specific, and process and system training materials and delivering them through live, virtual, or recorded sessions to support GCTO Regions. You will work collaboratively within the Monitoring Excellence team and engage with key stakeholders across GCTO to ensure training curricula are effective, through feedback and performance metrics, relevant, and aligned with business objectives.   Main Responsibilities <ul><li>Develop Training Materials: Create and maintain training content aligned with Global Clinical Development standards and Good Clinical Practices (GCPs) and End to End Monitoring activities, including role-based and therapeutic area-specific modules, monitoring processes, and systems. Maintain training materials in compliance with applicable SOPs, policies, and regulatory requirements. </li><li>Defines and contributes to the development of training strategies for GCTO Regions </li><li>Deliver Training Sessions: Conduct and deliver live, face to face, virtual, or recorded training for GCTO roles as required, ensuring engagement and knowledge retention, including train the trainer sessions as needed. </li><li>Collaborate Cross-Functionally: Work closely with our Company's R&D Learning & Development, subject matter experts, and process owners to design and implement effective training material. </li><li>Collaborates with our Company's R&D Learning & Development in the development and implementation of role-based training curricula. </li><li>Communications Support: Leads and develops communication materials (email, web content, presentations) to support training initiatives and business processes. </li><li>Monitor Training Effectiveness: Use metrics, surveys, and feedback tools to assess training impact and identify training needs, areas for improvement adjusting plans as appropriate to deliver improved performance. </li><li>Promote Best Practices: Implement and advocate for best practices in training design and delivery, ensuring alignment with company goals and quality standards. </li><li>Ensures that training maximizes competency with performance-based metrics tied to quality results. </li><li>Manages and oversees functional or cross-functional networks of training process owners/subject matter experts. </li><li>Collaborates with GCTO to increase visibility of local training, ensure alignment, avoid duplicity and globalize local training when applicable. </li><li>Provides back-up for Clinical Operations Educators in other Regions as needed. </li></ul> Qualifications, Skills & Experience Required Educational Requirements: <ul><li>Bachelor's degree in science (or equivalent e.g. nursing qualification) </li></ul>Preferred Educational Requirements:<ul><li>Advanced degree, (e.g., master's degree, M.D., PhD) </li></ul>Required Experience: <ul><li>5 years of experience in clinical research, with mandatory 2 years of CRA experience. </li><li>6 months of experience delivering training sessions, such as local or country-level training or subject matter expert (SME) training. </li></ul>Preferred Experience: <ul><li>1 year CRM experience </li></ul> Required Knowledge and skills: <ul><li>Strong knowledge of drug development and clinical trial processes, including relevant standards and documentation. </li><li>Familiarity with FDA Good Clinical Practices, ICH Guidelines, and other major regulatory agencies’ regulations and guidance. </li><li>Experience working in a hybrid environment with international cultural diversity. </li><li>Proficiency with learning technologies and platforms for delivering and tracking training. </li><li>Strong educational and coordination skills with demonstrated success in training delivery. </li><li>Excellent oral and written communication skills and ability to retain the attention of diverse audiences.</li><li>Flexibility to work across different time zones to collaborate globally and deliver training sessions as needed. </li><li> Demonstrated knowledge of how people learn and the ability to use various instructional approaches to enhance learning outcomes. </li><li>Demonstrated teamwork and leadership skills across organizational levels. </li><li>Ability to embrace change/improvement. </li><li>Demonstrated ability to analyze, interpret and solve problems. </li></ul>ResearchanddevelopmentGCTO eligibleforERPVETJOBSEBRGExtent of Travel: up to 40%   Note: remote positions, 3 openings: 1 based the Americas (North America or Latin America), 1 based in Europe and 1 based in Asia Pacific. Candidate can be based in any GCTO footprint countryCurrent Employees apply <a target=”_blank” href=” style=”text-align:inherit”>Current Contingent Workers apply <a target=”_blank” href=” style=”text-align:inherit”>US 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 <a href=”” target=”_blank”>click here</a> 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:<a href=”” target=”_blank”>EEOC Know Your Rights</a><a href=”” target=”_blank”>EEOC GINA Supplement</a>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.<a href=”” target=”_blank”>Learn more about your rights, including under California, Colorado and other US State Acts</a>U.S. Hybrid Work ModelEffective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday – Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.The salary range for this role is$139,600.00 – $219,700.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at <a href=”” target=”_blank”> can apply for this role through <a href=”” target=”_blank”>; (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.San 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: RegularRelocation:No relocationVISA Sponsorship:NoTravel Requirements:50%Flexible Work Arrangements:RemoteShift:Not IndicatedValid Driving License:YesHazardous Material(s):NoRequired Skills:Adaptability, Adaptability, Business Processes, Clinical Data Management, Clinical Research, Clinical Site Management, Clinical Supplies Management, Clinical Testing, Clinical Trial Management Processes, Clinical Trials Logistics, Communication Management, Cultural Diversity, Decision Making, Drug Development, Good Clinical Practice (GCP), Nursing, Patient Education, Quality Management, Quality Standards, Regulatory Compliance, Regulatory Requirements, Regulatory Submissions, Risk Based Monitoring, Risk Management, Strategic Planning {+ 4 more} Preferred Skills:Job Posting End Date:10/6/2025*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. Requisition ID:R366104

Company Job Link:

https://jobs.merck.com/us/en/job/R366104/Clinical-Operations-Educator-Remote

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