MERCK
Executive Director, Scientific Affairs, Rheumatology
MERCK, Washington, District of Columbia, us, 20022
Overview The Executive Director, Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic community to positively impact R&D strategy for new medicines and to improve patient outcomes. The EDSA leads a large investigator-initiated studies program in partnership with late-stage development teams in Medical Affairs while also supporting early-stage development teams. The role also partners with Medical Affairs leadership to develop the global Value Evidence And Medical (VEAM) Planning strategy across designated therapeutic areas. The EDSA has a key role at major Congresses, including facilitating daily debriefs, engaging with Scientific Leaders, and producing comprehensive Congress summary reports.
Qualifications, skills, and all relevant experience needed for this role can be found in the full description below. Primary Responsibilities
Leads our Company’s Investigator Initiated Studies program in assigned therapeutic areas ensuring scientific rigor Provides subject matter expertise for Product Development and Publications teams and facilitates cross-functional communication and collaboration in pursuit of our company’s R&D strategy Leads R&D activities and synthesizes competitive intelligence relevant to our company’s R&D strategy at key scientific congresses Leads our Company’s global scientific input forums to gain external scientific/clinical insights in support of our Company’s R&D strategy Sustains our Company’s scientific credibility and fosters and develops relationships with global leaders, major academic medical centers, and key professional societies and organizations through relevant bi-directional scientific exchange Guides development of consistent and accurate scientific content in support of our global field-based Medical Affairs teams and advises and supports them in providing global perspective in their interactions with external stakeholders Maintains personal expertise in the assigned disease area science in the context of advancing clinical and treatment paradigms Minimum Education Requirement
Medical degree (e.g., MD/MB BS or equivalent degree) Required Experience and Skills
8+ years of clinical leadership experience after completing postgraduate training in a related subspecialty Significant research experience as lead clinical investigator, specifically experience with investigator-initiated studies, concept assessment, and protocol review Proven ability to work in a complex matrix environment and effectively operate in a team-oriented structure Advanced facilitation and consultative skills Ability to effectively interact with internal and external stakeholders and to positively influence decision making at a senior level Excellent interpersonal communication (written and verbal) Results-oriented project management skills Preferred Experience and Skills
Higher scientific degree (e.g., PhD) in addition to medical degree Impactful publication record in a relevant therapeutic area, with international recognition Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld) Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld) 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 and 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, with Friday remote, unless business critical tasks require on-site presence. This model does not apply to field-based, facility-based, manufacturing-based, or research-based positions where work is located at a Company site; roles under a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position where remote work is not feasible. The salary range for this role is $304,800.00 - $479,800.00. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive benefits package and information can be found at the company compensation and benefits page. You can apply for this role through the company Careers site or Workday. The application deadline is stated on this posting. Additional Information We will consider qualified applicants in compliance with local laws. This posting is effective until the listed end date.
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Qualifications, skills, and all relevant experience needed for this role can be found in the full description below. Primary Responsibilities
Leads our Company’s Investigator Initiated Studies program in assigned therapeutic areas ensuring scientific rigor Provides subject matter expertise for Product Development and Publications teams and facilitates cross-functional communication and collaboration in pursuit of our company’s R&D strategy Leads R&D activities and synthesizes competitive intelligence relevant to our company’s R&D strategy at key scientific congresses Leads our Company’s global scientific input forums to gain external scientific/clinical insights in support of our Company’s R&D strategy Sustains our Company’s scientific credibility and fosters and develops relationships with global leaders, major academic medical centers, and key professional societies and organizations through relevant bi-directional scientific exchange Guides development of consistent and accurate scientific content in support of our global field-based Medical Affairs teams and advises and supports them in providing global perspective in their interactions with external stakeholders Maintains personal expertise in the assigned disease area science in the context of advancing clinical and treatment paradigms Minimum Education Requirement
Medical degree (e.g., MD/MB BS or equivalent degree) Required Experience and Skills
8+ years of clinical leadership experience after completing postgraduate training in a related subspecialty Significant research experience as lead clinical investigator, specifically experience with investigator-initiated studies, concept assessment, and protocol review Proven ability to work in a complex matrix environment and effectively operate in a team-oriented structure Advanced facilitation and consultative skills Ability to effectively interact with internal and external stakeholders and to positively influence decision making at a senior level Excellent interpersonal communication (written and verbal) Results-oriented project management skills Preferred Experience and Skills
Higher scientific degree (e.g., PhD) in addition to medical degree Impactful publication record in a relevant therapeutic area, with international recognition Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld) Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld) 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 and 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, with Friday remote, unless business critical tasks require on-site presence. This model does not apply to field-based, facility-based, manufacturing-based, or research-based positions where work is located at a Company site; roles under a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position where remote work is not feasible. The salary range for this role is $304,800.00 - $479,800.00. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive benefits package and information can be found at the company compensation and benefits page. You can apply for this role through the company Careers site or Workday. The application deadline is stated on this posting. Additional Information We will consider qualified applicants in compliance with local laws. This posting is effective until the listed end date.
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