Job Description
This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials.
Ophthalmology/Retina related experience required.
Job Responsibilities
- May have specific operational responsibilities for a single study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities).
- May be responsible for tracking study timelines using project management tools.
- Shares technical expertise with team members.
- May interact with internal and external stakeholders (e.g., study team, vendors, committees) in support of clinical trial objectives.
Core Skills
- Working knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
- Ability to manage multiple competing priorities with good planning, time management and prioritization skills
- Good understanding of the principles of project planning & project management
- Building analytical skills to drive operational milestones
- Interact with key stakeholders across department, division, and company. Role requires a proactive approach driving toward study goals.
- Problem solving, prioritization, conflict resolution, and critical thinking skills
- Solid communication, writing, and presentation skills
- Intermediate knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)
Education Experience
- Bachelor's Degree +2 years of pharmaceutical, clinical drug development, project management, and/or medical field experience
- OR Master's Degree +1 year of pharmaceutical, clinical drug development, project management, and/or medical field experience
- Degree in life sciences, preferred.
**Required Skills: **
Adaptability, Analytical Problem Solving, Biological Sciences, Clinical Research, Clinical Study Design, Clinical Trial Compliance, Clinical Trials, Clinical Trials Operations, Conflict Resolution, Data Management, Drug Development, Ethical Standards, Life Science, Medical Writing, Microsoft Outlook, Prioritization, Project Management, Project Planning, Regulatory Compliance, Regulatory Writing, Stakeholder Alignment, Stakeholder Relationship Management, Structured Content Management, Technical Writing, Written Communication
**Preferred Skills: **
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Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
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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:
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The salary range for this role is
$96,200.00 - $151,400.00
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.
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: **
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
06/1/2026
***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. **