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Associate Director, Global Scientific & Value Content (Hematology)

EyeBio

EyeBio

North Wales, PA, USA · Rahway, NJ, USA
USD 169,700-267,200 / year + Equity
Posted on Jul 15, 2025

Job Description

Role Summary

  • The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research.

  • This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans.

  • This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans.

  • This position develops and adapts GSVC plans for products and disease states aligned with V&I Plans.

  • This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the V&I organization.

Responsibilities and Primary Activities

  • Stakeholder Engagement: Develops and adapts the Value & Implementation Planning & Scientific Platform for GSVC Annual Product and Disease State Plans.

  • Content Development: Authors or works with vendors to create GSVC content aligned with Annual GSVC Plans, ensuring scientific accuracy and consistency.

  • Medical Insight Incorporation: Reviews and communicates GSVC content, integrating feedback from stakeholders.

  • Execution: Implements GSVC Plans, including medical information letters (MILs), verbal response documents (VRDs), slide decks, digital and modular content, innovative formats, and global congress medical booth materials, including staffing these booths.

  • Subject-Matter Expertise: Leads product- or disease area-related projects and initiatives, providing solutions for complex problems and mentoring junior staff.

  • Partnership: Collaborates with global stakeholders to ensure assets align with strategic medical plans and meet customer and internal needs. Acts as a medical scribe for global input meetings (GIMs) and provides an overview of the output of the meeting.

  • Process Improvement: Identifies gaps and leads initiatives such as creating departmental processes, standard operating procedures (SOPs), and cross-functional activities.

  • Cross-Functional Collaboration: Builds collaborative relationships across divisions and regions. Drives alignment of scientific content strategy and plans with other V&I partners, such as Publications, Clinical and Outcomes Research. Aims to ensure the timely availability of effective and compliant resources for Medical Information and Field Medical teams. Additionally, focuses on building collaborative relationships across divisions and regions to provide scientific resources that inform patient care, formulary, and treatment decisions. Leads and executes complex cross-functional initiatives that contribute to the strategy and objectives of GSVC and the broader GMSA stakeholders.

  • Training: Provides training to internal stakeholders on GSVC-developed disease and product content.

Additional Key and Enterprise Leadership Responsibilities:

  • Leads projects and solves complex problems: Oversees project management, providing solutions to complex issues, and guides junior staff through mentorship.

  • Collaborates globally: Works with international teams to align resources and assets with strategic medical plans.

  • Mentors new hires: Offers guidance and support to new hires, students and fellows, helping them acclimate and develop in their roles.

  • Prioritizes tasks and delivers high-quality work: Manages tasks efficiently, focusing on delivering high-quality work and contributing to team goals.

Required Qualifications, Skills and Experience Minimum

  • MD/PharmD/PhD, plus minimum 3 (three) years of relevant Medical Affairs (e.g., medical communications, medical information, medical liaison, publications) experience -or-

  • MSN, BS degree in Pharmacy, MS degree in Life Sciences plus minimum of 5 (five) years of Medical Affairs-related experience -or-

  • BS degree in Nursing or Life Sciences, plus minimum of 7 (seven) years of Medical Affairs-related experience.

  • Knowledge of the hematology oncology therapeutic area.

  • Exhibited leadership via initiatives, mentoring, process improvements, innovation.

  • Multi-tasking and problem-solving skills (solution-driven).

  • Excellent interpersonal and communication (written as well as oral) skills.

  • Organizational and prioritization skills.

Preferred

  • Advanced degree (MD, PharmD, PhD).

  • Experience with the development of Global or Regional Medical/Scientific Affairs Plans.

  • Ability to develop or deliver scientific content for purpose of scientific exchange with external customers.

  • Ability to negotiate with cross-functional teams.

  • Prior experience working across geographies with different regulation/compliance requirements.

  • Strong analytical skills and ability to translate strategy into action plans.

  • Demonstrated ability to work in a complex organization environment and able to effectively operate in a team-oriented structure as well as alone.

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

U.S. Hybrid Work Model

Effective 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

$169,700.00 - $267,200.00

This 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:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

25%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Hematology, Medical Affairs, Medical Communications, Medical Knowledge, Medical Review, Medical Writing, Pharmaceutical Medical Affairs, Project Management, Scientific Communications, Scientific Publications

Preferred Skills:

Job Posting End Date:

07/28/2025

*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.