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Global Therapeutics Jobs (NOW HIRING)

Parexel

Global Therapeutic Area Lead, Nephrology

$92K - $125K/yr

About Parexel Parexel is a leading global clinical development partner delivering insights-driven ... As a Therapeutic Area Lead, you will drive clinical excellence and medical oversight across complex ...

Parexel

$77K - $105K/yr

About Parexel Parexel is a leading global clinical development partner delivering insights-driven ... As a Therapeutic Area Lead, you will drive clinical excellence and medical oversight across complex ...

Parexel

Global Therapeutic Area Lead, Nephrology

$92K - $125K/yr

About Parexel Parexel is a leading global clinical development partner delivering insights-driven ... As a Therapeutic Area Lead, you will drive clinical excellence and medical oversight across complex ...

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Global Therapeutics information

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$62K

$125.5K

$326K

How much do global therapeutics jobs pay per year?

As of Sep 6, 2026, the average yearly pay for global therapeutics in the United States is $125,543.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $137,500.00 per year, depending on experience, location, and employer.

What is a global therapeutics professional?

Global Therapeutics professionals are experts who work in the development, regulation, and distribution of medical therapies on an international scale. They focus on bringing innovative treatments to global markets, ensuring that therapies meet international regulatory standards and address diverse patient needs. Their work often involves collaborating with cross-functional teams, navigating complex compliance requirements, and staying updated on advances in medical technology. The goal is to improve patient outcomes by making effective therapies accessible worldwide.

What are the key skills and qualifications needed to thrive as a global therapeutics specialist?

To thrive as a Global Therapeutics Specialist, you need a strong background in life sciences or pharmacy, in-depth knowledge of therapeutic areas, and relevant clinical or pharmaceutical experience. Familiarity with global regulatory standards, clinical trial management systems, and industry certifications such as GCP (Good Clinical Practice) are typically required. Excellent cross-cultural communication, project management, and analytical skills help professionals stand out in this role. These skills ensure effective coordination of global projects, regulatory compliance, and successful delivery of therapeutic solutions across diverse markets.

How does a global therapeutics professional typically collaborate with cross-functional teams to develop and launch new therapies?

In a Global Therapeutics role, professionals often work closely with research scientists, regulatory affairs, clinical development, and marketing teams to bring new therapies to market. Collaboration involves regular meetings to align on project goals, timelines, and regulatory requirements across different regions. Effective communication and adaptability are essential, as the team navigates complex global regulations and diverse patient needs. This collaborative environment provides opportunities to learn from various disciplines and contribute to impactful healthcare solutions.

What is the difference between Global Therapeutics vs Clinical Research Associate?

AspectGlobal TherapeuticsClinical Research Associate
Required CredentialsBachelor's in life sciences, relevant certificationsBachelor's in health sciences, clinical research certifications
Work EnvironmentPharmaceutical companies, biotech firms, global health organizationsClinical trial sites, hospitals, research organizations
Employer & Industry UsageUsed in global drug development and therapeutics companiesCommonly employed in clinical trial management and monitoring

Global Therapeutics professionals focus on developing and managing therapies on a global scale, often working with drug development teams. Clinical Research Associates primarily oversee clinical trial processes at trial sites. While both roles require similar educational backgrounds and certifications, their work environments and responsibilities differ significantly, with Global Therapeutics roles centered on therapeutic development and Clinical Research Associates on trial execution and monitoring.

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What cities are hiring for Global Therapeutics jobs?

Cities with the most Global Therapeutics job openings:

What states have the most Global Therapeutics jobs?

States with the most job openings for Global Therapeutics jobs include:

What job categories do people searching Global Therapeutics jobs look for?

The top searched job categories for Global Therapeutics jobs are:

Global Therapeutics jobs near you
Infographic showing various Global Therapeutics job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 11% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $125,543 per year, or $60.4 per hour.

Quality Engineer, Quality Systems

Merz Therapeutics

Raleigh, NC • On-site

$63K - $82K/yr

Full-time

Posted 3 days ago

New

Job description

Step into the future with us at Merz Therapeutics, where our family roots meet a bold new vision. Together, we're embarking on a transformative journey, blending time-honored traditions with exciting new products.
As a private, family-owned company, we have the liberty and support to make decisions for ourselves, our customers and the patients we serve. We pride ourselves on building an inclusive culture where there is room to celebrate individual growth with the ability to contribute to a common good as a collaborative team. Our mission is grounded in a long-term view of making a difference for the common good, while growing together as a family.
If you're looking to immerse yourself in a passionate team rooted in community, connection and camaraderie, then we're looking for YOU! #IAmMerz
Are you ready to galvanize a team around a culture of care, putting patients first to spark change?
The Quality Engineer, Quality Systems will provide support for quality system functions with a focus on technical product quality complaint management. Responsibilities include complaint intake, data processing, case tracking, complaint returns, investigations, case closeout, and customer responses. This role will also support the company's quality training and document control systems, including document lifecycle management, employee training administration, and assistance to departments in authoring and maintaining controlled documents.
Essential Duties and Responsibilities of this job
  1. Technical Product Quality Complaints
    • Complaint intake
    • Data processing
    • Case tracking
    • Complaint returns and product replacements or credits
    • Complaint investigations for local products
    • Case closeout and customer responses.
    • Perform monthly reconciliations of complaint data received from external partners and internal stakeholders to ensure the completeness, accuracy, and regulatory compliance of complaint records and associated quality system documentation.
    • Monitor the Quality Complaint Inbox daily.
    • Assist with the preparation and implementation of Quality Assurance policies and procedures.
    • Complaints trending and metrics reporting.
    • Communicate with patients, customers, and other relevant parties to obtain and document information necessary to support technical product quality complaint investigations and ensure complete and accurate complaint records.
  2. Document Control / Training
    • Document lifecycle management (SOP creation, review, approval)
    • Assist departments with authoring SOPs, understanding document and training processes, monitoring training assignments, and following up on overdue training.
    • Assist with preparing and implementing Quality Assurance policies and procedures.
    • Track employee training completion and follow up with managers regarding overdue training, training assignments, and document routing activities.
    • Monitor the Document Control Inbox daily.
    • Serve as a liaison between Merz Tx and the Global Team, facilitating effective communication, collaboration, and alignment on quality system activities and initiatives.
  3. Deviations and CAPAs
    • Support the administration of Quality System processes related to deviations, CAPAs, and associated tracking and implementation activities.
  4. Quality Systems and Continuous Improvement
    • Support Quality System processes and initiatives to maintain compliance with company procedures and applicable regulatory requirements.
    • Assist with quality metrics, trend analysis, and Quality Management Review activities.
    • Participate in continuous improvement projects and quality system enhancement initiatives.
  5. Inspections and internal audits
    • Assist with Quality System inspections, regulatory audits, and internal audits.
  6. Quality Assurance Diligence
    • Support adherence to Quality Assurance performance indicators and quality system requirements.
    • Participate in quality team meetings and Quality Management Review activities.
    • Collaborate with Quality, Regulatory Affairs, Safety, and other cross-functional teams.
    • Participate in quality improvement initiatives and cross-functional projects.
    • Maintain compliance with the Global Therapeutics Quality Management System.
    • Support Merz Therapeutics U.S. and Canadian product recall activities, including process execution, communications, and reporting requirements.
  7. Additional responsibilities as assigned: supporting local leadership in any quality objectives as applicable, staying up to date on SOP reading/training requirements and notifying manager of regulatory compliance about overdue training.
Job Requirements
Education & Certifications
  • Bachelors degree in Science or Engineering, or equivalent experience, preferred.
Professional Experience
  • Minimum 3 years of experience in the pharmaceutical industry is required, preferably within a Quality Assurance or Quality Systems function.
  • Experience working in and with different people and organizational cultures, supporting people with diverse backgrounds, attitudes and cultural differences.
  • A quality certification such as ASQ Certified Quality Engineer is considered an asset.
  • Experience creating and maintaining quality metrics dashboards, analyzing trends, and communicating performance data through graphical presentations using tools such as Power BI, Tableau, Excel, or equivalent business intelligence platforms is considered an asset.
Knowledge, Skills & Abilities
  • Working knowledge of GMP, GDP, and Canadian Food and Drug Regulations.
  • Ability to communicate with Regulatory and Quality personnel.
  • Must be proficient in Microsoft Office applications including Word, Excel and PowerPoint.
  • Prior experience working with electronic quality management systems such as JIRA, MasterControl, TrackWise, Veeva, etc., is considered an asset.
  • Experience with quality systems records, including CAPA, Deviations, Change Controls and complaint handling.
  • Strong interpersonal, collaborative, organizational skills and ability to multi-task.
  • Fluency in English and excellent verbal and written communication skills.
  • Commitment to quality practices and principles.
Travel Requirements
Travel is minimal for this role. Occasional travel may be required for training, conferences, or visits to the Canadian site.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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