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Array Biopharma Jobs (NOW HIRING)

Ardelyx

Commercial Legal Counsel

Waltham, MA · On-site

$214K - $250K/yr

Description Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment ... wide array of legal issues pertaining to Ardelyx. The Commercial Legal Counsel will report to the ...

Ardelyx

Commercial Legal Counsel

Waltham, MA · On-site

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches ... wide array of legal issues pertaining to Ardelyx. The Commercial Legal Counsel will report to the ...

Ardelyx

Commercial Legal Counsel

Waltham, MA · On-site

$214K - $250K/yr

Description Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment ... wide array of legal issues pertaining to Ardelyx. The Commercial Legal Counsel will report to the ...

Ardelyx

Commercial Legal Counsel

Waltham, MA

$214K - $250K/yr

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches ... wide array of legal issues pertaining to Ardelyx. The Commercial Legal Counsel will report to the ...

Ardelyx

Commercial Legal Counsel

Waltham, MA

$214K - $250K/yr

Description Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment ... wide array of legal issues pertaining to Ardelyx. The Commercial Legal Counsel will report to the ...

Ardelyx

Commercial Legal Counsel

Waltham, MA

$214K - $250K/yr

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches ... wide array of legal issues pertaining to Ardelyx. The Commercial Legal Counsel will report to the ...

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How much do array biopharma jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for array biopharma in the United States is $31.13, according to ZipRecruiter salary data. Most workers in this role earn between $30.77 and $31.49 per hour, depending on experience, location, and employer.

What key skills and qualifications are needed to thrive at Array Biopharma, and why are they important?

To thrive at Array Biopharma, professionals typically need a strong background in pharmaceutical sciences, molecular biology, or chemistry, often with an advanced degree in a related field. Familiarity with drug discovery platforms, laboratory information management systems (LIMS), and relevant regulatory standards such as GLP and GMP is important. Excellent problem-solving skills, teamwork, and effective communication set individuals apart in collaborative research environments. These skills and qualifications are crucial for driving innovation, ensuring compliance, and contributing to successful drug development projects.

What collaborative opportunities can I expect when working at Array BioPharma as a research scientist?

At Array BioPharma, research scientists frequently collaborate with multidisciplinary teams, including medicinal chemists, biologists, and data analysts, to drive innovative drug discovery projects. You can expect to participate in regular cross-functional meetings, share data, and contribute to joint problem-solving sessions. This collaborative environment not only accelerates project timelines but also provides valuable learning experiences and exposure to different aspects of pharmaceutical research. Such collaboration is key to Array's dynamic and fast-paced culture, fostering both professional growth and scientific advancement.

What is Array BioPharma and what do they do?

Array BioPharma is a biopharmaceutical company that focuses on the discovery, development, and commercialization of targeted small molecule drugs to treat cancer and other diseases. Founded in 1998 and headquartered in Boulder, Colorado, Array has developed several innovative therapies, including drugs for melanoma and colorectal cancer. The company is known for its expertise in chemistry and drug design, and it has collaborated with major pharmaceutical firms to advance its research. In 2019, Array BioPharma was acquired by Pfizer, further expanding its impact in oncology therapeutics.

Is Array BioPharma owned by Pfizer?

Array BioPharma was acquired by Pfizer in 2019, making it a part of Pfizer's portfolio. The acquisition included the rights to develop and commercialize Array's cancer treatments, and employees may work within Pfizer's broader organization. Job seekers should review current company structures for specific roles and responsibilities.

What jobs in the US pay 300,000 a year?

High-paying jobs that can reach or exceed $300,000 annually include roles such as senior physicians, specialized surgeons, anesthesiologists, and certain executive positions like CEOs and investment bankers. These roles typically require advanced degrees, extensive experience, and often involve high levels of responsibility and expertise in their fields.

What is the difference between Array Biopharma vs Clinical Research Associate?

AspectArray BiopharmaClinical Research Associate
Required CredentialsBachelor's in life sciences, relevant certificationsBachelor's in health sciences, clinical research certifications
Work EnvironmentBiotech labs, pharmaceutical companiesClinical trial sites, hospitals, research organizations
Employer & Industry UsageBiotech firms, pharmaceutical companiesContract research organizations, pharma companies
Common Search & ComparisonYesYes

Array Biopharma professionals focus on drug discovery and development within biotech and pharmaceutical companies, often working in laboratory settings. Clinical Research Associates (CRAs) oversee clinical trials, ensuring compliance and data integrity at trial sites. While both roles are essential in the drug development process, Array Biopharma roles are more lab-based, whereas CRAs are field-based, working directly with clinical trial sites.

More about Array Biopharma jobs
What states have the most Array Biopharma jobs? States with the most job openings for Array Biopharma jobs include:
What job categories do people searching Array Biopharma jobs look for? The top searched job categories for Array Biopharma jobs are:
Array Biopharma jobs near you
Infographic showing various Array Biopharma job openings in the United States as of May 2026, with employment types broken down into 36% Full Time, and 64% Part Time. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $64,760 per year, or $31.1 per hour.
CMC Regulatory Affairs Project Manager - Foster City, CA - Contract

CMC Regulatory Affairs Project Manager - Foster City, CA - Contract

ObjectWin Technology, Inc.

Foster City, CA • On-site

Contractor

Posted 20 days ago

Job description

Company Description
ObjectWin provides global workforce solutions to meet current and future business demands of our customers. Our services include, various workforce solutions, SOW based projects and fulltime resource deployments. We serve our customers both nationally and globally.
Job Description
  • Job Title: CMC Regulatory Affairs Project Manager
  • Duration: 6 Months
  • Job Location: 333 Lakeside Drive, Foster City, CA 94404

No Remote, No C2C - USC/GC holders only
Description: The CMC Regulatory Affairs Project Manager will be responsible for tracking the status of key filings for clinical and commercial programs for all global markets. The Project Manager will communicate with the cross functional CMC teams on small molecule and biologics submissions tracking. The Project Manager will attend CMC regulatory meetings and will be responsible for maintaining timelines, meeting minutes, action items, resource plans and other project documents.
Job Responsibilities:
  • Facilitate communication of regulatory activities across CMC Sub-Teams and Senior Management
  • Work on an improved tool for the regulatory department to track submissions
  • Generate metrics on regulatory submissions and approvals across a wide-array of submission subtypes.
  • Tracking of regulatory filings for clinical and commercial programs for all global markets
  • Develop and manage detailed project timelines for regulatory activities
  • Monitors project execution and adjusts plans
  • Facilitates communication and documentation of regulatory activities across project teams and senior management
  • Collaborates with the team to resolve issues and organizes team to execute on the corrective actions
  • Ensures project work complies with established practices, policies and processes

Qualifications
  • Minimum 6 years of relevant experience and a BA or BS or 4 + years of relevant experience and a MS or MBA. Relevant experience consists of work in cross functional biopharmaceutical /pharmaceutical CMC development, GMP and regulatory affairs
  • Excellent organizational skills, capable of setting priorities and delivering on commitments, while managing high workload
  • Strong communication skills; written and verbal including oral presentation skills
  • Experience in regulatory CMC project management is preferred
  • In-depth knowledge and skill with Microsoft Project, Excel, PowerPoint, Word, Visio, SharePoint and other reporting/tracking tools

Additional Information
If this position be of interest to you, please contact me directly at 832-485-3662

Apply