Associate Director, Clinical Scientist, Ophthalmology

HireLifeScience; Boston (MA); On-site; USD 142,000 - 224,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) retirement plan

Paid time off

Job summary

Merck & Co., Inc. is seeking a Senior Clinical Scientist to drive scientific planning, strategy, and execution of Phase 1–4 ophthalmology trials.

You will collaborate with global clinical directors, study managers, and other specialists to lead scientific activities across the trial lifecycle. You will oversee protocol execution, lead the clinical science effort, and partner with Medical Writers on regulatory documentation, while mentoring team members and coordinating with study leaders to meet

Qualifications

• Bachelor's Degree +8 years of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology.
• OR master's degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology
• OR PhD/PharmD Degree +4 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
• Degree in life sciences, preferred.
• Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Documentation, Clinical Trials Monitoring, Good Clinical Practice (GCP), Life Science, Pharmaceutical Sciences, Strategic Thinking, Study Design

Responsibilities

• Clinical/scientific execution of clinical protocol(s).
• Lead clinical scientist on the clinical trial team.
• Collaborates with the Medical Writer on clinical/scientific and regulatory documents.
• Partners with Study Manager on study deliverables.
• Participates in the set up and design during study start up (e.g., database set up)
• Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations
• Builds talent and capabilities of direct/indirect team members through coaching and development
• May include management of direct reports including resource assignment and performance management
• May serve as subject matter expert and participate on process improvement teams

Skills

Clinical Development

Clinical Research

Clinical Trial Documentation

GCP & ICH

Study Design

Regulatory Collaboration

Leadership

Communication

Education

Bachelor's Degree +8 years of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology

Or master's degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology

Or PhD/PharmD Degree +4 year of pharmaceutical, clinical drug development, project management, and/or medical field experience

Degree in life sciences, preferred

Job description

Job Description

This position drives scientific planning, strategy, and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global cross functional team members including clinical directors and study managers to lead/support clinical trial scientific activities.

Job Responsibilities

• Responsible for the clinical/scientific execution of clinical protocol(s).
• Serves as the lead clinical scientist on the clinical trial team.
• Collaborates with the Medical Writer on clinical/scientific and regulatory documents.
• Partners with Study Manager on study deliverables.
• Participates in the set up and design during study start up (e.g., database set up)
• Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director.
• Builds talent and capabilities of direct/indirect team members through proactive coaching, mentoring and development opportunities.
• May include management of direct reports including assignment of resources, professional development, and performance management.
• May serve as a subject matter expert and/or participate on process improvement teams.

Core Skills

Demonstrated ability to drive and manage scientific activities on clinical protocols. This position may represent the company through external partnerships, collaborations, and key strategic engagements. This includes the ability to:

• Apply strong knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
• Manage multiple competing priorities with good planning, time management, and prioritization skills
• Advanced analytical skills with the ability to interpret clinical trial data and synthesize conclusions
• Interact with key stakeholders across department, division, and company. Role requires a proactive approach, strategic thinking and leadership driving toward study goals.
• Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division
• Demonstrated ability to effectively delegate and assign activities to meet the business needs
• Problem solving, prioritization, conflict resolution, and critical thinking skills
• Build team capabilities through proactive coaching
• Advanced communication, technical writing, and presentation skills

Education/Experience Preferred

• Bachelor's Degree +8 years of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology

• OR master's degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience in ophthalmology
• OR PhD/PharmD Degree +4 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
• Degree in life sciences, preferred.

Required Skills

Clinical Development, Clinical Research, Clinical Sciences, Clinical Trial Documentation, Clinical Trials Monitoring, Good Clinical Practice (GCP), Life Science, Pharmaceutical Sciences, Strategic Thinking, Study Design

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.

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.

Salary Range

$142,400.00 - $224,100.00

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.

Benefits

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 .

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

10%

Flexible Work Arrangements

Not Applicable

Shift

1st - Day

Valid Driving License

No

Hazardous Material(s)

No

Job Posting End Date

10/14/2026

*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

R418851