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Cro Pharmaceutical Jobs (NOW HIRING)

Senior Biostatistician

Princeton, NJ ยท On-site

$130K - $160K/yr

Prior experience in a CRO/pharmaceutical environment, required * Oncology clinical trials preferred * Experience with phase I trials preferred Skills and Competencies * Expertise in statistical ...

Senior Biostatistician

Princeton, NJ ยท On-site

$130K - $160K/yr

Prior experience in a CRO/pharmaceutical environment, required * Oncology clinical trials preferred * Experience with phase I trials preferred Skills and Competencies * Expertise in statistical ...

Senior Biostatistician

Princeton, NJ ยท On-site

$130K - $160K/yr

Prior experience in a CRO/pharmaceutical environment, required * Oncology clinical trials preferred * Experience with phase I trials preferred Skills and Competencies * Expertise in statistical ...

Senior Biostatistician

Princeton, NJ ยท On-site

$130K - $160K/yr

Prior experience in a CRO/pharmaceutical environment, required * Oncology clinical trials preferred * Experience with phase I trials preferred Skills and Competencies * Expertise in statistical ...

IT Project Manager

Portsmouth, NH ยท On-site

$100K - $118K/yr

... CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is ...

Showing results 41-60

Cro Pharmaceutical information

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How much do cro pharmaceutical jobs pay per hour?

As of Sep 14, 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 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.

Is CRO a good career?

A career as a CRO (Contract Research Organization) professional involves working in clinical research, often requiring knowledge of regulatory standards, data management, and trial processes. It can offer opportunities in the pharmaceutical and biotech industries with roles in project management, monitoring, and data analysis. The field generally provides stable employment with potential for advancement and specialization.
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:

Infographic showing various Cro Pharmaceutical job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Senior Biostatistician

Princeton, NJ โ€ข On-site

$130K - $160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago


Job description

Who We Are
Celebrating 40+ years!
Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials.
What You'll Do
As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.
Your primary responsibilities will include the following:
  • Ensures successful completion of high-quality statistical deliverables
  • Writes and/or reviews statistical sections of protocols
  • Assists in protocol study design (determines sample sizes for all phases of trials)
  • Writes Statistical Analysis Plans (SAPs)
  • Writes Tables, Listings and Figures Plans (TLF Plans)
  • Reviews and/or designs Case Report Forms (CRFs)
  • Reviews and/or writes randomization and blinding plans
  • Reviews and/or writes charters for Data Monitoring Committees (DMCs)
  • Provides SAS code for statistical models
  • Validates/performs SAS programming for key data analyses
  • Performs quality control on derived variables being analyzed
  • Interprets results from analysis
  • Maintains documentation
  • Reviews Clinical Study Reports (CSR)
  • Keeps abreast of statistical literature/design

What You Need
Level of Education
  • Master's degree in Biostatistics or equivalent, required

Prior Experience
  • 5+ years of experience in clinical biostatistics, required
  • Prior experience in a CRO/pharmaceutical environment, required
  • Oncology clinical trials preferred
  • Experience with phase I trials preferred

Skills and Competencies
  • Expertise in statistical concepts and design
  • Understands the investigational drug development process
  • Demonstrates ability to build and maintain effective relationships with others
  • Strong communication, organizational and decision-making skills
  • High level of agility and diplomacy
  • Must be able to anticipate challenges and project risks and proactively implement solutions
  • Strong time management and effective planning skills
  • Knowledge of Standard Operating Procedures
  • Working knowledge of FDA and ICH guidelines
  • Working knowledge of MS Office and Outlook

What We Offer
At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), very competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for this position ranges from $130,000-$160,000. The actual salary offer will be based on a number of factors, including but not limited to the candidate's qualifications, experience, skills, and competencies for the role.
This position is not eligible for relocation or company provided sponsorship.
Theradex is an Equal Opportunity Employer.