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Director Merck Clinical Trials Jobs (NOW HIRING)

  • Medical

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... clinical trials led by Dr. Wahl. The relevant individual will also work on diagnostic imaging ... With the Administrative Director and Medical Director, strategically plans and implements plans for ...

Clinical Trials Manager

Foster City, CA

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

... direct impact. We believe every employee deserves a great leader. People Leaders are the ... Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in ...

Clinical Trials Manager

Foster City, CA

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

... direct impact. We believe every employee deserves a great leader. People Leaders are the ... Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in ...

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Director Merck Clinical Trials information

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How much do director merck clinical trials jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for director merck clinical trials in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What is the difference between Director Merck Clinical Trials vs Clinical Project Manager Merck?

AspectDirector Merck Clinical TrialsClinical Project Manager Merck
ResponsibilitiesOversees multiple clinical trials, strategic planning, team leadership, and high-level decision makingManages individual clinical trial projects, coordinates activities, and ensures timelines and budgets are met
Required CredentialsAdvanced degree (PhD, MD, or PharmD), extensive clinical research experience, leadership skillsBachelor's or Master's in life sciences, clinical research experience, project management skills
Work EnvironmentStrategic, leadership-focused, often in corporate or senior management settingsOperational, team-oriented, often in clinical trial sites or project teams

The main difference between a Director Merck Clinical Trials and a Clinical Project Manager Merck lies in scope and responsibilities. The director focuses on strategic oversight and leadership across multiple trials, while the project manager handles day-to-day project execution. Both roles require clinical research experience, but the director typically has more advanced credentials and a broader leadership role.

What cities are hiring for Director Merck Clinical Trials jobs?

Cities with the most Director Merck Clinical Trials job openings:

What are the most commonly searched types of Merck Clinical Trials jobs?

The most popular types of Merck Clinical Trials jobs are:

What states have the most Director Merck Clinical Trials jobs?

States with the most job openings for Director Merck Clinical Trials jobs include:

Clinical Trials Safety Data Manager

Integrated Resources INC

Cambridge, MA

Full-time

Re-posted 4 days ago


Job description

Company Description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Client: Direct Client

Location: Cambridge, MA

Job Title: Safety Data Collection Manager 

Duration: 1 year


Responsibilities 

Responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval Clinical Studies globally.

Supports the Senior Manager, Safety Data Collection Clinical Trials and is responsible for setting the safety operations strategy, establishing the safety report collection standards and processes, and ensuring they are implemented and executed consistently throughout all Pre and Post-Marketing Clinical Studies globally. 

Clinical Trials Associate will provide partner / vendor oversight in relation to Clinical Trial safety report collection and will collaborate with other functions (e.g., Clinical Operations, Medical Affairs, Data Management, Medical Writing, Regulatory, Biostatistics, and others ) to ensure consistency with regulations and with departmental goals and objectives. 

Support Senior Manager, Safety Data Collection, Clinical Trials with setting the safety operation strategy and establishing the safety report collection standards and processes for Pre and Post-approval Clinical Studies globally Senior Manager, Safety Data Collection, Clinical Trials. 

Execute the development, maintenance and implementation of Controlled documents (SOPs), data handling conventions and other process documents for Clinical Trials and Post-Marketing Clinical Studies. 

Safety operational content and processes for Clinical Trial and Post-Marketing Clinical Study tools for report collection such as protocols, CRFs, SAE forms, Pregnancy forms.

Tools and processes for database requirements and configurations to enable safety-related activities during studies.

Training requirements and materials for Clinical Trial safety report collection. 

Report metrics and KPIs for Clinical Trial safety report collection Senior Manager, Safety Data Collection, Clinical Trials.

Oversee and ensure study safety operational requirements are operationalized Senior Manager, Safety Data Collection, Clinical Trials.

Support the following Strategic Partner / vendor oversight activities, in conjunction with relevant functions (such as Global Clinical Operations) in relation to Clinical Trial safety report collection. 

Provide functional support / input to set up partner and vendor relationship (e.g., business requirements, vendor selection, contract details, vendor oversight / safety management plans).

Support onboarding and ongoing maintenance of partner and vendor status to perform work (e.g., access, training, technology set-up). 

Provide ongoing support of partners and vendors (e.g., questions, issues, meetings). 

Conduct partner oversight and performance management on contracted work (e.g., monitoring reports, quality evaluations, annual meetings) Senior Manager, Safety Data Collection, Clinical Trials.

Communicates on PV legislation and regulatory commitments across the organization and externally Senior Manager, Safety Data Collection, Clinical Trials. 

Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing Clinical Studies during audits / inspections Senior Manager, Safety Data Collection, Clinical Trials.

Qualifications

Qualification


Minimum of Bachelor's level degree in nursing, pharmacy, or other health care related profession or life sciences required.


Master's or Doctorate level degree in health care related profession preferred.  


4+ years in drug safety/Pharmacovigilance in pharmaceutical industry setting or the equivalent. 


Experience interacting with clinical third parties (e.g., contract research organizations) preferred. 


Knowledgeable in Pharmacovigilance and GCP legislation required. 


Direct experience in GXP compliant quality systems preferred.




Note: Out of state candidates are also entertained who are willing to relocate at their own expenses.



Additional Information


Feel free to forward my email to your friends/colleagues who might be available




Thanks!!!




Warm Regards,


Amrit Singh


Clinical Recruiter


Integrated Resources, Inc.


IT REHAB CLINICAL NURSING


Tel: (732) 429 1634 (Direct)


Ext: (732) 549 2030 x (212) 


Fax: (732) 549 5549


http://www.irionline.com


Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012, 2013 & 2014 (8th Year)


Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70


https://www.linkedin.com/company/46970?trk=prof-exp-company-name




Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996