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Merck Associate Director Jobs in Colorado (NOW HIRING)

The Associate Director Oncology Treatment Site Lead (TSL) is the primary field-based point of ... Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does ...

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Merck Associate Director information

See Colorado salary details

$32.1K

$108K

$181.9K

How much do merck associate director jobs pay per year?

As of Aug 22, 2026, the average yearly pay for merck associate director in Colorado is $108,020.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,600.00 and $148,300.00 per year, depending on experience, location, and employer.

What does a Merck Associate Director do?

A Merck Associate Director typically oversees teams or projects within a specific department, such as research, marketing, or regulatory affairs. They are responsible for developing strategies, ensuring compliance with company and regulatory standards, and achieving departmental goals. Associate Directors often manage budgets, mentor staff, and collaborate with other leaders to drive business objectives. Their role is critical in advancing Merck’s mission and maintaining high performance across their area of responsibility.

What are the key skills and qualifications needed to thrive as a Merck Associate Director?

To thrive as a Merck Associate Director, you typically need a relevant advanced degree (such as in life sciences, business, or a related field), substantial industry experience, and strong leadership capabilities. Familiarity with regulatory compliance systems, data analysis tools, and project management software is often required, along with any specialized certifications pertinent to the business area. Strategic thinking, effective communication, and the ability to lead cross-functional teams are crucial soft skills in this role. These competencies are vital for driving business objectives, ensuring regulatory adherence, and fostering effective team collaboration within a complex corporate environment.

What are some common challenges faced by a Merck Associate Director, and how can candidates prepare to address them?

As an Associate Director at Merck, one common challenge is balancing strategic leadership with hands-on project management, especially in a fast-paced, highly regulated environment. You'll often need to coordinate cross-functional teams and align diverse stakeholders, so strong communication and organizational skills are key. Candidates should be prepared to navigate shifting priorities, regulatory changes, and tight deadlines while ensuring alignment with Merck’s mission and compliance standards. Proactively building knowledge in pharmaceutical regulations and stakeholder management can help you succeed in this role.

What is the difference between Merck Associate Director vs Merck Senior Manager?

CriteriaMerck Associate DirectorMerck Senior Manager
Required credentialsAdvanced degree (MBA, PhD), relevant industry experienceBachelor's or Master's degree, significant industry experience
Work environmentStrategic leadership, cross-functional collaborationOperational management, team oversight
Employer and industry usageCommon in pharmaceutical and biotech sectorsWidely used in similar sectors for mid-to-senior roles
Search and comparison intentHigh overlap in responsibilities and qualificationsSimilar level, often compared for career progression

The Merck Associate Director typically holds a more strategic, leadership-focused role requiring advanced degrees and extensive industry experience. In contrast, the Merck Senior Manager is more operational, overseeing teams and projects. Both roles are integral in pharmaceutical companies, with the Associate Director often preparing for executive leadership, while the Senior Manager manages day-to-day functions.

Is a Merck associate director a high position?

An Associate Director at Merck is considered a senior management role, typically ranking above managers and below directors or vice presidents. It involves significant leadership responsibilities, strategic planning, and often requires advanced industry experience and expertise. This position is generally regarded as a high-level role within the company hierarchy.

What cities in Colorado are hiring for Merck Associate Director jobs?

Cities in Colorado with the most Merck Associate Director job openings:

Infographic showing various Merck Associate Director job openings in Colorado as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $108,020 per year, or $51.9 per hour.

Associate Director, Oncology Treatment Site Lead - Northwest Territory (CO, ID, MT, NV, OR, UT, WA,

Merck & Co.

On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job DescriptionOur Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval.The Associate Director Oncology Treatment Site Lead (TSL) is the primary field-based point of contact for operational information and support for product treatment sites. This role educates and supports sites so that they can consistently execute the end-to-end product operational journey-from onboarding and readiness through ordering workflow execution and steady-state operations. TSLs will help support sites by educating them about necessary processes, answering questions about operational issues, and supporting a reliable, seamless experience across the treatment journey. The TSL is focused on operational and process support, and not clinical treatment information. --This role requires strong knowledge of treatment-site operations, the ability to navigate complex cross-functional workflows, and the ability to align internal and external stakeholders to support reliable end-to-end site execution as well as timely issue resolution.This is a field-based, customer-facing, non-demand generating and non-promotional role. The Associate Director Oncology Treatment Site Lead (TSL) role will have responsibility for accounts in the Northwest geography, which includes, CO, ID, MT, NV, OR, UT, WA and WY. The candidate must reside in the designated geographic territory.Primary Activities & Responsibilities include and are not limited to the following:Lead the onboarding and readiness support process for product treatment sites, ensuring treatment sites are educated on the workflow, system setup, and operational requirementsDeliver process-focused education for site stakeholders using approved resources to support initial site implementation and ongoing operational supportHelp ensure treatment sites have the operational capabilities and knowledge required for consistent execution of the product's end-to-end treatment journeyServe as the product operational subject matter expert for your assigned treatment sites and provide support regarding the product process, operations, and logistics.Act as the primary point of contact for operational issues, triaging and appropriately addressing issues through cross-functional coordination and defined processesAppropriately collaborate with cross-functional oncology field teams (as approved) to support coordinated, compliant engagement and a consistent experience for product treatment sites.Build trusted business relationships with site operational leaders by delivering consistent, reliable, and responsive operational support.Utilize our company generated data and dashboards to assess appropriate site operational metrics (as approved) and identify opportunities for operational improvement.Synthesize site feedback and process insights to help HQ team enhance communication, operational workflows, resources and education.Qualifications:Bachelor's degree requiredMinimum of 5 years of relevant experience in healthcare or life sciences, including sales, account management, or provider operations/administrationStrong understanding of the healthcare ecosystemProven track record of working with provider organizations and operational stakeholders to implement workflows for complex therapiesAbility to operate effectively in "white space" environments with evolving processes, unclear paths, and multiple dependenciesStrong operational problem-solving skills, including identifying process friction points, diagnosing root causes, and coordinating next steps with appropriate stakeholdersAbility to build and develop meaningful customer relationships with operational stakeholders at treatment sites-Excellent interpersonal and communication skills, internally and externally, with ability to interact with individuals from a variety of cultures and disciplinesStrong leadership skills and ability to collaborate in cross-functional, matrix organizations-Ability to travel ~50%Valid driver's license.PreferredExperience supporting site activation/readiness and operational support for advanced therapies (e.g. cell therapies, gene therapies, radioligand therapies)Experience working with complex oncology workflowsExperience working with large oncology systems and navigating multiple stakeholder groups across a single enterpriseRequired Skills: Account Management, Account Management, Business Management, Business Relationship Building, Cell and Gene Therapy, Collaboration, Communication, Cross-Functional Collaboration, Cross-Functional Teamwork, Cytometry, Cytopathology, Immunotherapy, Logistics Management, Messenger RNA, Onboarding, Oncology, Patient Treatment, Product Lifecycle, Project Implementations, Radioimmunoassay (RIA), Radiopharmaceuticals, Service Readiness, Site Activation, Site Operations, Stakeholder Engagement {+ 1 more}Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE 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 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 Rights EEOC GINA Supplement• 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 The salary range for this role is $190,800.00 - $300,300.00This 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 https://jobs.merck.com/us/en/compensation-and-benefits .You can apply for this role through https://jobs.merck.com/us/en (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 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.-Employee Status: RegularRelocation:No relocationVISA Sponsorship:No Travel Requirements: 50%Flexible Work Arrangements:RemoteShift:1st - DayValid Driving License:YesHazardous Material(s):NAJob Posting End Date:09/17/2026 *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. Requisition ID:R411668 Salary: . Date posted: 08/20/2026

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