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Cro Pharmaceutical Jobs (NOW HIRING)

ttg Talent Solutions

Senior Project Manager

Raleigh, NC

$130K - $140K/yr

The ideal candidate brings extensive project management experience within the Clinical Trials, CRO, Pharmaceutical, Biotechnology, or Life Sciences industry , with demonstrated success leading ...

Katalyst CRO

CSV Engineer

Redwood City, CA · On-site

Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate ...

Us tech Solutions

CRO Partner Manager Duration: 12Months Location: Whippany, NJ 07981 Alliance Management is part of ... BA or BS in a pharmaceutical development related field Requirements: * 5-7 years' experience in ...

Us tech Solutions

CRO Partner Manager Duration: 12Months Location: Whippany, NJ 07981 Alliance Management is part of ... BA or BS in a pharmaceutical development related field Requirements: * 5-7 years' experience in ...

Frontage Laboratories

Associate QC Specialist

Exton, PA · On-site

Experience * 0-3 years of experience in a bioanalytical laboratory, biomarker research, or quality control role in a CRO, pharmaceutical, or biotechnology environment. * Experience with GLP-regulated ...

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How much do cro pharmaceutical jobs pay per hour?

As of Jul 12, 2026, the average hourly pay for cro pharmaceutical in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What jobs pay $500,000 a year in the US?

In the pharmaceutical industry, senior executive roles such as Chief Medical Officer, Chief Scientific Officer, or Vice President of R&D can earn $500,000 or more annually, especially with bonuses and stock options. These positions typically require extensive experience, advanced degrees, and leadership skills in research, development, or management environments.

What is the difference between Cro Pharmaceutical vs Clinical Research Associate?

AspectCro PharmaceuticalClinical Research Associate
CredentialsTypically requires a degree in pharmacy, life sciences, or related fieldRequires a degree in life sciences, healthcare, or related field; certifications like CCRA are common
Work EnvironmentPharmaceutical companies, research labs, manufacturing facilitiesClinical trial sites, hospitals, research organizations
Industry UsageUsed in pharmaceutical manufacturing, quality control, and regulatory complianceInvolved in monitoring clinical trials, ensuring protocol adherence

While Cro Pharmaceutical focuses on manufacturing, quality assurance, and regulatory aspects within the pharmaceutical industry, Clinical Research Associates primarily oversee clinical trial processes. Both roles require scientific backgrounds and industry experience but differ in daily responsibilities and work settings.

What does a CRO do in pharma?

A CRO (Contract Research Organization) in pharma manages and conducts clinical trials on behalf of pharmaceutical companies. They handle tasks such as study design, patient recruitment, data collection, and regulatory compliance, often using specialized software and adhering to Good Clinical Practice (GCP) standards.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior executive roles such as Chief Medical Officer (CMO) or Vice President of Research and Development typically have the highest salaries. These positions require extensive experience, advanced degrees, and leadership skills, and they often oversee large teams and strategic decision-making.

Is it better to work for a CRO or pharmaceutical company?

Working as a CRO professional often involves project-based roles with flexible schedules and exposure to multiple clients, while pharmaceutical companies typically offer more stable employment, specialized roles, and a focus on drug development and manufacturing. The choice depends on career goals, preferred work environment, and desired skill development, such as regulatory knowledge or clinical trial management.
More about Cro Pharmaceutical jobs
What cities are hiring for Cro Pharmaceutical jobs? Cities with the most Cro Pharmaceutical job openings:
What states have the most Cro Pharmaceutical jobs? States with the most job openings for Cro Pharmaceutical jobs include:
What job categories do people searching Cro Pharmaceutical jobs look for? The top searched job categories for Cro Pharmaceutical jobs are:
Cro Pharmaceutical jobs near you
Infographic showing various Cro Pharmaceutical job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 3% Part Time, and 2% Contract. Highlights an 71% Physical, 2% Hybrid, and 27% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.
Senior Project Manager

Senior Project Manager

ttg Talent Solutions

Raleigh, NC

$130K - $140K/yr

Full-time

Posted 11 days ago

Job description

Senior Project Manager
Location: Miami, Florida or Raleigh, North Carolina
Work Arrangement: On-site / Hybrid (based on business needs)
Schedule: Full-Time
Employment Type: Direct Hire
Position Summary
Our client, a leading organization within the Life Sciences industry, is seeking an experienced Senior Project Manager to lead complex, strategic, and cross-functional initiatives from project initiation through successful implementation.
This highly visible role is responsible for managing customer-facing and internal projects that support operational excellence, new service implementations, clinical trial logistics programs, process improvement initiatives, digital transformation efforts, and organizational growth. The Senior Project Manager will partner with customers, vendors, and cross-functional teams to ensure projects are delivered on time, within scope, within budget, and in compliance with established quality and governance standards.
The ideal candidate brings extensive project management experience within the Clinical Trials, CRO, Pharmaceutical, Biotechnology, or Life Sciences industry, with demonstrated success leading projects in highly regulated environments.
Key Responsibilities
  • Project Leadership & Delivery
  • Lead complex strategic projects from initiation through successful completion.
  • Define project scope, objectives, deliverables, schedules, budgets, and resource plans.
  • Develop and maintain comprehensive project documentation, including project plans, timelines, risk registers, governance documentation, and status reports.
  • Monitor project milestones, critical paths, dependencies, and overall project performance.
  • Identify project risks and develop mitigation and contingency strategies.
  • Manage project changes through formal governance and change control processes.
  • Ensure project deliverables meet quality standards and stakeholder expectations.
  • Provide regular project updates to executive leadership, customers, and project stakeholders.
Stakeholder & Customer Management
  • Serve as the primary point of contact for customers, vendors, and internal stakeholders throughout the project lifecycle.
  • Build strong relationships with executive-level stakeholders and cross-functional teams.
  • Facilitate project meetings, governance reviews, steering committee sessions, and project workshops.
  • Manage customer expectations while ensuring alignment with project objectives.
  • Support customer onboarding, implementation, and operational transition activities.
Process Improvement & Operational Excellence
  • Lead End-to-End (E2E) process mapping, analysis, and optimization initiatives.
  • Develop and maintain RACI matrices to define ownership and accountability.
  • Identify opportunities to improve operational efficiency through process redesign and continuous improvement.
  • Apply project management methodologies including Agile, Waterfall, Lean, Six Sigma, DMAIC, or other best practices as appropriate.
Strategic Initiatives
  • Lead strategic initiatives including:
  • New customer implementations
  • New service launches
  • Clinical trial logistics programs
  • Technology implementations and system integrations
  • Digital transformation initiatives
  • New operational start-ups
  • Facility launch projects
  • Geographic expansion initiatives
Additionally, this role will:
  • Manage third-party vendors and external service providers throughout project execution.
  • Support RFI, RFP, RFQ, and vendor evaluation processes when applicable.

Required Qualifications
  • Bachelor's Degree in Engineering, Supply Chain, Business Administration, Information Technology, Life Sciences, or a related discipline.
  • Minimum of five (5) years of project management experience leading complex, cross-functional projects.
  • Current PMP, PRINCE2, Scrum Master, Agile, or equivalent Project Management certification.
  • Demonstrated experience managing customer-facing projects within the Clinical Trials, CRO, Pharmaceutical, Biotechnology, or Life Sciences industry.
  • Clinical Trials industry experience is required and considered a non-negotiable qualification.
  • Proven experience leading operational improvement, technology implementation, business transformation, or large-scale implementation projects.
  • Experience leading End-to-End (E2E) process analysis and process improvement initiatives.
  • Strong customer-facing experience working with executive-level stakeholders.
  • Experience managing external vendors and third-party partners.
  • Excellent written and verbal communication skills.
  • Exceptional organizational, planning, problem-solving, and leadership skills.

Preferred Qualifications
  • Experience supporting clinical trial logistics, depot operations, or clinical supply chain activities.
  • Experience supporting global clinical trial operations.
  • Knowledge of regulated Life Sciences environments, including GxP, GDP, and ICH guidelines.
  • Experience within logistics or supply chain operations.
  • Experience managing international or multi-country projects.

Language Requirements
  • English: Professional written and verbal proficiency required.
  • Spanish: Preferred but not required.

Work Location
This position may be based in:
  • Miami, Florida
  • Raleigh, North Carolina
Candidates should be comfortable collaborating with customers, colleagues, and stakeholders located across multiple regions and time zones.
ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees.
At ttg, "We believe in making a difference One Person at a Time," ttg OPT.
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