Director, Site Relationship Managers (REMOTE)
MSDAbout the role
Job Description
This role serves as a key internal and external representative for US Country Operations to facilitate country level implementation of key initiatives impacting sites, develop and support oversight of key metrics to assess partner site collaborations and serves as an interface with internal global site network and external site forums/ professional societies.
The role will provide a strategy for the SRMs, work with the Country CRD and SMM Directors to identify key institutions and establish a strategy for sites as center of excellence in support of a Therapeutic Area (TA) needs.
Primary responsibilities for the role include:
Drives innovation and initiatives to improve site relationships, including new company technologies, and tools to support sites
Fosters relationships with internal and external stakeholders in developing and maintaining key institutions and center of excellence sites
Drives process improvements, innovative solutions to help reduce barriers and mitigate risks that directly impacts investigator sites and requires multiple internal stakeholder interfaces
Engaging with industry stakeholders to build industry awareness and develop our company's company brand and reputation
Maintains deep understanding of US site landscape
Manage direct reports including performance plans and development plans. Oversee performance management, career development of staff and effectively manage performance issues.
Work closely with country leadership to assess priority sites and issue escalation, strategic partner relationships.
Create, promote and direct a strategy whereupon the functions of the SRM role is identified by sites/institutions as their central point of contact for our company's relationships.
Establish procedures and processes, key metrics, criteria for assessing key sites
Extent of Travel:
50%
Qualifications, Skills & Experience
Education:
Bachelor’s Degree required
Experience and Skills:
Minimum 12 years of experience within the Pharmaceutical industry
Minimum 10 years in clinical trial operations
Deep knowledge and understanding of Clinical Development Processes & Procedures
Significant project management and business process improvement experience, with demonstrated record of accomplishments
Familiarity with the clinical operations of pharmaceutical development from an industry perspective; well developed and effective team facilitation and leadership skills; able to establish cooperative team environments
Data analytics
Networking and Partnerships
Business Savviness
#eligibleforerp
ResearchandDevelopmentGCTO
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
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We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
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