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Drug Development Project Manager Jobs in Exton, PA

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 ...

We offer a wide range of manufacturing, packaging, and research and development services. Our ... This is the meaning behind "Transforming Drug Delivery - Transforming Lives." Our Culture When it ...

Pharma IT, GxP Project, PMP Certification Domain Experience Working knowledge of ICH Guidelines and ... Broad knowledge of drug development process and client needs Prior experience working on regulatory ...

This position will initially be responsible for managing a mobile development project consisting of 3 to 5 resources, with a career path towards a senior leadership roles within Acumen Solutions.

This position will initially be responsible for managing a mobile development project consisting of 3 to 5 resources, with a career path towards a senior leadership roles within Acumen Solutions.

Showing results 21-40

Drug Development Project Manager information

See Exton, PA salary details

$41.5K

$91.2K

$137.1K

How much do drug development project manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for drug development project manager in Exton, PA is $91,246.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,800.00 and $104,700.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a drug development project manager, and why are they important?

A Drug Development Project Manager requires expertise in pharmaceutical sciences, regulatory requirements, and project management, often supported by a relevant degree and PMP certification. Familiarity with project management tools (like MS Project or Smartsheet), clinical trial management systems, and documentation platforms is essential. Excellent leadership, strategic communication, and problem-solving abilities help navigate complex timelines and cross-functional teams. These skills ensure efficient project execution, regulatory compliance, and successful advancement of drug candidates through development phases.

What does a drug development project manager do?

A Drug Development Project Manager oversees and coordinates all aspects of pharmaceutical product development, from early research through clinical trials to regulatory approval and market launch. They manage cross-functional teams, timelines, budgets, and communications to ensure projects meet scientific, regulatory, and business goals. These professionals play a critical role in identifying risks, troubleshooting issues, and ensuring compliance with industry standards. Their work helps bring new therapies to market efficiently and safely.

What is the difference between Drug Development Project Manager vs Clinical Research Associate?

AspectDrug Development Project ManagerClinical Research Associate
CredentialsBachelor's/Master's in life sciences, PMP certification often preferredBachelor's in life sciences, clinical research certification beneficial
Work EnvironmentCoordinates multiple teams across drug development phasesMonitors clinical trial sites and ensures protocol compliance
Industry UsageUsed in pharmaceutical and biotech companies during drug developmentPrimarily in clinical trial sites and CROs

The Drug Development Project Manager oversees the entire drug development process, coordinating teams and managing timelines. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites to ensure compliance and data integrity. Both roles are essential in the drug development pipeline but differ in scope and responsibilities.

What are some common challenges faced by drug development project managers, and how can these be managed effectively?

Drug Development Project Managers often encounter challenges such as coordinating cross-functional teams, managing shifting regulatory requirements, and ensuring projects stay on schedule and within budget. Effective communication and proactive risk management are essential to navigate these complexities. Building strong relationships with stakeholders and maintaining transparent project plans can help address issues early and keep development efforts aligned with company goals.
What job categories do people searching Drug Development Project Manager jobs in Exton, PA look for? The top searched job categories for Drug Development Project Manager jobs in Exton, PA are:
What cities near Exton, PA are hiring for Drug Development Project Manager jobs? Cities near Exton, PA with the most Drug Development Project Manager job openings:
Infographic showing various Drug Development Project Manager job openings in Exton, PA as of June 2026, with employment types broken down into 1% As Needed, 89% Full Time, 5% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $91,246 per year, or $43.9 per hour.

Study Manager, Clinical Operations

MSD

North Wales, PA • On-site

$96K - $151K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago


Job description

Job Description

Job Summary:

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.

Job Responsibilities:

  • May have specific operations responsibilities for a single study or across multiple studies (e.g. operational deliverables, clinical & ancillary supplies planning, lab specimen tracking, status update reports, study close-out 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 f 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.

clinicaltrialjobs

Required Skills:

Clinical Research, Clinical Study Design, Clinical Trial Compliance, Clinical Trials, Clinical Trials Operations, Data Management, Ethical Standards, Project Management, Regulatory Compliance, Stakeholder Alignment, Structured Content Management

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:

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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.

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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:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

08/4/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.