Senior Director, Clinical Development Antibacterials, Antifungals, CMV & Covid 19

Job Description

Job description

Anti-infective drug development has been our core mission for over 80 years. Our Clinical Research group is at the forefront of global healthcare through research and innovation to combat established and emerging pathogens. Through clinical trials we ensure that our existing and pipeline products are developed to produce safe effective and innovative medicines and we work with cross-functional colleagues in Global Medical and Scientific Affairs and Global Policy to ensure timely access to our medicines.

The Senior Director has primary responsibility for protocol development and medical/scientific oversight of clinical research studies involving investigational or marketed drugs in the infectious diseases therapeutic area. The individual will participate in all phases of the clinical trial process (mainly Phase 2-3) including study design medical monitoring and medical/scientific interpretation of study analysesregulatory reporting and publication. The individual will apply an in-depth understanding of the disease under study and drug pharmacology to the infectious disease therapeutic areas clinical development strategy and the implementation of short- and long-term research objectives. They will provide internal scientific leadership for cross-functional areas supporting clinical development and external leadership through interaction with key scientific leaders.

Role may be remote

Specifically the Senior Director may be responsible for:

Planning clinical trials (design operational plans) based on the clinical development strategies for investigational or marketed infectious disease drugs

Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed infectious disease drugs

Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications clinical study reports or publications

Participation in internal and joint internal/external research project teams relevant to the development of investigational drugs and the further study of marketed drugs

Developing clinical development strategies for investigational or marketed infectious disease drugs

Presenting study data and program strategic plans to internal governance committees for endorsement and key program milestones

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within their area of expertise including new scientific findings and research methodologies

Establishing communications with prominent clinical investigators in their particular field of interest particularly those scientifically and operationally strong investigators who can assist in the development of our companys investigational and marketed drugs

Attending appropriate scientific meetings to maintain their competency and to maintain awareness of research activities in their area of responsibility.

To accomplish these goals the Senior Director may:

Author detailed development documents and presentations for internal and external audiences

Author scientific publications

Facilitate collaborations with external researchers around the world

Travel on company business up to about 10% of the time to manage future or ongoing clinical research projects.

Qualifications

Education:

M.D or M.D./Ph.D preferably with demonstrated expertise in infectious diseases

Eligibility for medical licensure and board certification desirable

An individual with postgraduate program yielding a PharmD degree and demonstrated expertise in clinical practice or clinical research may also be considered for the position

Requirements:

Industry experience in clinical research and drug development (at least 5 years)

Demonstrated success in overseeing clinical studies and protocols

Demonstrated record of scientific scholarship and achievement

Experience in clinical medicine

Excellent communication skills both verbal and written

Strong interpersonal skills as well as the ability to function in a team environment and leadership experience

Preferred

Background in infectious diseases clinical research and drug development

Prior experience with registrational trials and filing with major health authorities

Required Skills:

Clinical Development Clinical Judgment Clinical Medicine Clinical Research Management Clinical Trial Compliance Clinical Trial Development Clinical Trials Data Analysis Decision Making Drug Development Ethical Standards Infectious Disease Infectious Disease Research Intellectual Curiosity Interdisciplinary Problem Solving Medical Research Mentorship Protocol Development Regulatory Compliance Regulatory Reporting Scientific Consulting Scientific Publications Strategic Planning Vaccinology Veterinary Medicine

Preferred Skills:

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US and Puerto Rico Residents Only:

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The salary range for this role is

$282200.00 - $444200.00

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 employees 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 can apply for this role through (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

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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:

Domestic

VISA Sponsorship:

Yes

Travel Requirements:

10%

Flexible Work Arrangements:

Remote

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

07/13/2026

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