Onsite
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.
PhD/PharmD/OD +2 years Ophthalmology/Retina Related experience in industry or academia required.
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
Bachelor's Degree +9 years of pharmaceutical, clinical drug development, project management, and/or medical field experience
OR Master's Degree +6 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
OR PhD/PharmD Degree +2 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
Degree in life sciences, preferred.
Required Skills:
Adaptability, Adaptability, Analytical Problem Solving, Biological Sciences, Clinical Data Interpretation, Clinical Data Management, Clinical Operations, Clinical Research, Clinical Site Management, Clinical Study Design, Clinical Study Management, Clinical Trial Compliance, Clinical Trials, Clinical Trials Operations, Conflict Resolution, Data Analysis, Drug Development, Ethical Standards, Good Clinical Practice (GCP), Health Literacy, Life Science, Medical Writing, People Management, Prioritization, Stakeholder Alignment {+ 1 more}Preferred Skills:
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:
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
The salary range for this role is
$142,400.00 - $224,100.00This 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:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
1st - DayValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
05/29/2026*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.
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