We spend a great deal of time ensuring that people are compensated appropriately and aim to provide highly competitive pay levels over the long term

Compensation programs

For employees outside the U.S., time off and leave benefits are based on local laws and market practices.

Vacation, holidays, & year-end shutdown

INSPIRE is our worldwide recognition program designed to help create a culture of acknowledgement and appreciation.

Global recognition program

We offer health, life, disability, and business travel insurance that help protect our employees from the financial impact of unforeseen circumstances

Health, life, disability, & business travel insurance

We foster an array of flexible work arrangements that will help you succeed personally and professionally.

Global flexible work arrangements

We want our employees to be healthy and happy offering them the optimal working conditions with ergonomic workplaces

Safe & healthy workplaces

Merck Sharp & Dohme

For more than 130 years, we’ve brought hope to humanity through the development of important medicines and vaccines. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities.&nbsp;
We aspire to be the premier research-intensive biopharmaceutical company. We’re at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.&nbsp;

Source: MSD Site

Who We Are

Patients first
We're all accountable for delivering high quality products and services. We aspire to improve the health and wellness of people and animals worldwide and to expand access to our medicines and vaccines. All of our actions must be measured against our responsibility to those who use or need our products.
&nbsp;
<h4>Respect for people</h4>
Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity, safety and teamwork of our employees. We work to create an environment of mutual respect, inclusion and accountability. We reward commitment and performance and are responsive to the needs of our employees and their families.
&nbsp;
<h4>Ethics and integrity</h4>
We're committed to the highest standards of ethics and integrity. We're responsible to all of our stakeholders: employees, patients, customers, distributors and suppliers, shareholders, and the communities we serve worldwide. We do not take professional or ethical shortcuts.
&nbsp;
<h4>Innovation and scientific excellence</h4>
We're dedicated to the highest standard of innovation and scientific excellence. Our research is guided by a commitment to improving health and quality of life. We strive to identify and meet the most critical needs of patients and customers through continuous innovation across all areas of our business.

Source: MSD Site

Our Values

Job Description<div><div><ul><li>Join the premier biopharmaceutical company&nbsp;that has been in the Asia Pacific (AP) for over 60 years.&nbsp;</li></ul></div><div><ul><li>Be part of best-in-class Medical Affairs Team and be at the center of innovation and excellence in execution.&nbsp;</li></ul></div><div>Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry leaders ensuring the scientific value of our products is understood. We connect, communicate and train internal employees to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate our portfolio.&nbsp;</div><div>What will you do in this role:&nbsp;</div></div><div><div><ul><li>Lead the Regional Scientific Operations Sub Team to provide operational support for assigning a variety related activities across AP countries.&nbsp;</li></ul></div><div><ul><li>Global/regional/local medical &amp; scientific affairs studies (including Local Data Generation (LDG), HECON, Post Approval Studies/Researches, Company Investigator Studies Program &nbsp;and In Scope Research Types (interventional or non-interventional), and Pre-License Patient Access (PLPA) Programs across ≥2 markets. Assist line manager in constructing and managing the Regional Scientific Operations team of in-sourced personnel. Train local field medicals/study leads on subjects related to study operations and corresponding SOPs.&nbsp;</li></ul></div><div>&nbsp;</div><div>Scientific Operations management expectations include:&nbsp;</div><div><ul><li>Develop, maintain, and monitor project plans, project schedules, budgets, and expenditures in compliance with local regulations and company SOPs and Policy.&nbsp;</li></ul></div><div><ul><li>Organize and participate in project meetings (e.g., captures meeting minutes, tracks action items, contribute own perspectives, etc.),&nbsp;</li></ul></div><div><ul><li>Proactively discuss with study leads and line managers to assess project risks and issues and provide solutions where applicable,&nbsp;</li></ul></div><div><ul><li>Track project progress and provide project updates/summaries,&nbsp;</li></ul></div><div><ul><li>Navigate internal processes and procedures, including compliance and finance, to ensure compliant execution of assigned projects,&nbsp;&nbsp;</li></ul></div><div><ul><li>Ensure projects adhere to frameworks and all documentation is maintained appropriately for each project.&nbsp;</li></ul></div><div><ul><li>Publication Tracking.&nbsp; &nbsp;</li></ul></div><div>&nbsp;</div><div>Medical Scientific Operations Management - Study Activities &nbsp;</div><div><ul><li>Lead and/or participate in the team to work with study lead to plan, initiate, conduct and manage a series of local/regional/global planned non-interventional studies with Global Medical Scientific Affairs and related Staffs:&nbsp;</li></ul></div><div><ul><li>Lead and/or participate the team to plan, initiate, conduct and manage a series of local/regional planned Company&nbsp;Investigator Studies Program&nbsp;and In Scope Research Types (interventional or non-interventional) with Global Medical Scientific Affairs and related Staffs:&nbsp;</li></ul></div><div><ul><li>Timely track the publication status of GMSA studies (submission time, acceptance/rejection, conference, journal).&nbsp;</li></ul></div><div><ul><li>Publication includes conference poster, abstract, oral presentation and manuscript published in peer-reviewed journal.&nbsp;</li></ul></div><div><ul><li>Regularly track and provide status updates to study leads and country medical directors, execute all study related administrative tasks, such as execute contracting and study payment, arrange study material allocation and delivery, arrange SIV/PI meetings, budget management and monthly accrual, etc.&nbsp;</li></ul></div><div>&nbsp;</div><div>Medical Scientific Operations Management - PreLicense Patient Access Programs (PLPA)&nbsp;</div><div><ul><li>Work with project lead to Implement and track GMSA-Owned PreLicense Patient Access Programs (PLPA) and ensure the execution quality, under the supervision of manager&nbsp;</li></ul></div><div><ul><li>Conduct AE/PQC reconciliation process with GPV team to align with Global Pharmacovigilance Policy/SOP.&nbsp;</li></ul></div><div><ul><li>Execute Good Documentation Practice through out for all GMSA studies, Events &amp; activities and PLPA programs.&nbsp;</li></ul></div><div><ul><li>Involve or/and conduct internal audit, inspections, and other quality assurance activities.&nbsp;</li></ul></div><div><ul><li>Provide recommendation or trainings for continuous improvement, risk management control and knowledge transfer of Medical Scientific Affairs Projects within the company.&nbsp;</li></ul></div><div><ul><li>Support Medical Scientific Affairs in driving operational excellence and help build the Regional Scientific Operations team structure.&nbsp; &nbsp;</li></ul></div><div>What You Should Have&nbsp;</div><div><ul><li>Bachelor’s degree or Master’s Degree in pharmacy or related healthcare or scientific discipline.&nbsp;</li></ul></div><div><ul><li>Experience 8 years+ experience within clinical/observational research or equivalent experience; 3 years+ of experience in project management, vendor management and budget-planning.&nbsp;</li></ul></div><div><ul><li>Demonstrated pharmaceutical industry experience with a proven track record of leading large, complex, multi-stakeholder projects.&nbsp;</li></ul></div><div>&nbsp;</div><div>Core:&nbsp;</div><div><ul><li>Strong project management skills and sense of urgency&nbsp;</li></ul></div><div><ul><li>Have ability to deal with ambiguity&nbsp;</li></ul></div><div><ul><li>Clinical study execution related knowledge, including but not limited to GCP, GPP, IRB submission, HA submission, site initiation/close out, site management, liaise with vendors, budget planning/management, study drug import, specimen export, etc.&nbsp;</li></ul></div><div><ul><li>Strong interpersonal, verbal, and written communication skills to work with medical and/or scientific teams&nbsp;</li></ul></div><div><ul><li>Ability to independently handle multiple projects and priorities simultaneously and function in a fast-paced environment&nbsp;</li></ul></div><div><ul><li>Experience working effectively both independently and as part of a team&nbsp;</li></ul></div><div><ul><li>Ability to quickly and comprehensively learn about new subject areas and environments&nbsp;</li></ul></div><div><ul><li>Self-motivation, flexibility, resourcefulness, and problem-solving capabilities, passion for science&nbsp;</li></ul></div><div>&nbsp;</div></div><div>Who we are:&nbsp;</div><div>We are known as Merck &amp; Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.&nbsp;</div><div>&nbsp;What we look for:&nbsp;</div><div>Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.&nbsp;</div>Current Employees apply <a target="_blank" href="https://wd5.myworkday.com/msd/d/task/1422$6687.htmld">HERE</a>Current Contingent Workers apply <a target="_blank" href="https://wd5.myworkday.com/msd/d/task/1422$4020.htmld">HERE</a>Search Firm Representatives Please Read Carefully&nbsp; Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; 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. &nbsp;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.&nbsp;Employee Status: RegularRelocation:VISA Sponsorship:Travel Requirements:Flexible Work Arrangements:HybridShift:Valid Driving License:Hazardous Material(s):Required Skills:Adaptability, Adaptability, Business Intelligence (BI) Reporting, Clinical Project Management, Communication, Data Analysis, Decision Making, Internal Auditing, Knowledge Management, Management Process, Medical Affairs, Medical Knowledge, Medicines Australia Code of Conduct, Meeting Organization, Microsoft Office, Microsoft PowerPoint, Military Medicine, Pharmaceutical Regulatory Compliance, Pharmacovigilance, Project Management, Project Planning, Project Risks, Quality Assurance Processes, Requisition Management, Stakeholder Engagement {+ 5 more}&nbsp;Preferred Skills:Job Posting End Date:06/28/2025*A job posting is effective until 11:59:59PM on the day BEFORE&nbsp;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:R351951

This job is for a Senior Scientific Operations Manager at a leading biopharmaceutical company. You might like this job because you&#x27;ll drive innovation in healthcare, leading projects that improve patient access and understanding of vital medicines.

Job Description

-Join the premier biopharmaceutical company that has been in the Asia Pacific (AP) for over 60 years. 

-Be part of best-in-class Medical Affairs Team and be at the center of innovation and excellence in execution. Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry leaders ensuring the scientific value of our products is understood. We connect, communicate and train internal employees to ensure a th...

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Company Profile

Merck Sharp & Dohme