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Full Time Cra Pharmaceutical Jobs (NOW HIRING)

Vanguard Clinical

Clinical Research Associate (Pool)

CA · Remote

$90K - $130K/yr

We welcome interest from both full-time employees and independent consultants for this role ... The Clinical Research Associate (CRA) will execute monitoring responsibilities for clinical trials ...

Adecco

Clinical Research Associate

Waltham, MA · On-site

$30 - $32/hr

Monday-Friday | Full-Time Business Hours Position Summary Adecco Healthcare & Life Sciences is ... CRO, pharmaceutical, biotechnology, or academic research environments Why Work with Adecco Health ...

Shifamed

Sr. Field Clinical Specialist

Los Gatos, CA · On-site

$120K - $175K/yr

Collaborate with the clinical monitors, in-house CRA during site selection, qualification and ... The base salary range for this full-time position is between $120,000 to $175,000 + equity ...

Shifamed

Sr. Field Clinical Specialist

Los Gatos, CA · On-site

$120K - $175K/yr

Collaborate with the clinical monitors, in-house CRA during site selection, qualification and ... The base salary range for this full-time position is between $120,000 to $175,000 + equity ...

Sitero LLC

Director, Business Development

Raleigh, NC · On-site

$150K - $175K/yr

... Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ... EMPLOYMENT TYPE: Full Time, Permanent COMMITMENTS: * Standard Hours 40 hours per week, one hour ...

Sitero LLC

Director, Business Development

Raleigh, NC · Remote

$150K - $175K/yr

... Pharmaceutical / Biotech organization is required * Previous experience as a CRA, CTM, or in ... EMPLOYMENT TYPE: Full Time, Permanent COMMITMENTS: * Standard Hours 40 hours per week, one hour ...

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Full Time Cra Pharmaceutical information

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$11K

$79.4K

$137.5K

How much do full time cra pharmaceutical jobs pay per year?

As of Jul 30, 2026, the average yearly pay for full time cra pharmaceutical in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time Clinical Research Associate (CRA) in the pharmaceutical industry, and why are they important?

To thrive as a Full Time CRA in pharmaceuticals, you need a bachelor's degree in life sciences, strong knowledge of Good Clinical Practice (GCP), and experience in clinical trial monitoring. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and relevant certifications such as ACRP or SOCRA are typically required. Excellent organizational skills, attention to detail, and strong communication abilities help build relationships with site staff and ensure protocol compliance. These competencies are crucial for maintaining data integrity, regulatory adherence, and the overall success of clinical research projects.

What is the difference between Full Time Cra Pharmaceutical vs Full Time Clinical Research Associate?

AspectFull Time Cra PharmaceuticalFull Time Clinical Research Associate
CredentialsBachelor's degree in life sciences, relevant certificationsBachelor's degree in health sciences, clinical research certifications
Work EnvironmentPharmaceutical companies, clinical trial sitesClinical trial sites, CROs, pharmaceutical firms
Industry UsagePrimarily in pharmaceutical R&DAcross clinical research organizations and pharma
Job FocusMonitoring clinical trials in pharma settingsMonitoring and managing clinical trial progress

Both roles involve clinical trial monitoring, but Full Time Cra Pharmaceutical typically focuses on pharmaceutical company projects, while Full Time Clinical Research Associate may work across various organizations. The credentials and work environments are similar, making them closely related roles in clinical research.

Is CRA better than CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are different roles in clinical trials; CRAs typically oversee multiple sites and monitor study progress, while CRCs manage day-to-day trial activities at a single site. Both roles require knowledge of Good Clinical Practice (GCP) and may involve different certifications, but neither is inherently better—each has distinct responsibilities suited to different career paths in clinical research.

Is it hard to get a CRA job?

Securing a CRA (Clinical Research Associate) position can be competitive, often requiring relevant experience, a degree in life sciences or related fields, and certifications such as the CCRA. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve chances of employment.

How much does a senior CRA make at Iqvia?

A senior Clinical Research Associate (CRA) at IQVIA typically earns between $80,000 and $110,000 annually, depending on experience, location, and certifications. The role involves monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What are the most common challenges faced by full-time Clinical Research Associates (CRAs) in the pharmaceutical industry?

Full-time CRAs in the pharmaceutical sector often encounter challenges such as managing multiple clinical trial sites simultaneously, ensuring regulatory compliance, and maintaining consistent communication with site staff. Balancing travel requirements with reporting deadlines and frequent data monitoring can also be demanding. Effective organization, adaptability, and relationship-building skills are essential for success, as CRAs serve as a critical link between sponsors, investigators, and regulatory bodies.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior roles such as Vice President of Research and Development or Chief Scientific Officer tend to be the highest paying positions, often earning six-figure salaries. These roles require extensive experience, advanced degrees, and leadership skills, and they oversee drug development, regulatory strategies, and company direction.

What are Full Time CRA Pharmaceutical jobs?

Full Time CRA (Clinical Research Associate) Pharmaceutical jobs involve monitoring and managing clinical trials for pharmaceutical companies to ensure compliance with regulatory standards and study protocols. CRAs are responsible for visiting clinical trial sites, ensuring accurate data collection, and safeguarding the well-being of study participants. They work closely with site staff, sponsors, and regulatory bodies to ensure that trials are conducted ethically and efficiently. Full-time positions typically require a strong background in life sciences, attention to detail, and excellent organizational skills.
More about Full Time Cra Pharmaceutical jobs
What cities are hiring for Full Time Cra Pharmaceutical jobs? Cities with the most Full Time Cra Pharmaceutical job openings:
What are the most commonly searched types of Cra Pharmaceutical jobs? The most popular types of Cra Pharmaceutical jobs are:
What states have the most Full Time Cra Pharmaceutical jobs? States with the most job openings for Full Time Cra Pharmaceutical jobs include:
What job categories do people searching Full Time Cra Pharmaceutical jobs look for? The top searched job categories for Full Time Cra Pharmaceutical jobs are:
Full Time Cra Pharmaceutical jobs near you
Infographic showing various Full Time Cra Pharmaceutical job openings in the United States as of July 2026, with employment types broken down into 34% Locum Tenens, 59% Full Time, 2% Part Time, 1% Contract, and 4% Summer. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate II

Corcept Therapeutics

Redwood City, CA • On-site

$129K - $152K/yr

Full-time

Re-posted 2 days ago

Job description

For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases.
Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com.
The Clinical Research Associate (CRA) II monitors clinical study activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols. This is an onsite role.
Responsibilities
  • Supervises study preparation, site preparation and the in clinic phases directly or through a CRO for assigned studies
  • Ensures that GCPs and Corcept clinical SOPs are met throughout the clinical program
  • Acts as liaison with clinical vendors and other functional area team members to meet project goals
  • Coordinates cross-functional components of the clinical trials process such as drug product supplies, etc.
  • Participates in the preparation and negotiation of clinical trial agreements and study budgets
  • Produces RFPs and participates in the evaluation and negotiation of bids from prospective vendors
  • Shares protocol writing with the medical director and biostatistician and ensures that all boilerplate requirements are met
  • Drafts informed consent forms ensuring that they are in agreement with the protocols
  • Participates in the development of study related documents including CRFs, study manuals and related documents
  • Coordinates all study start up activities, potentially with and through the CRO
  • Participates in site management and monitors study sites in the field with the CRO or independently on an as needed basis
  • Collects, reviews and tracks essential trial documents
  • Provides the clinical team and the program team with information regarding CRO and clinical site performance and recommend remediation when needed
  • Participates in study management to ensure study project goals are met
  • Other duties as assigned

Preferred Education & Experience
  • BS / BA (science or health care field) or RN
  • 3+ years' experience as a CRA or field monitor at least some of which was in a big pharma or big CRO setting
  • Additional experience in the pharmaceutical industry is desirable

Preferred Skills & Experience
  • Knowledge of the clinical trials process, the application of SOPs, and medical terminology
  • Therapeutic and protocol knowledge
  • Excellent verbal and written communication skills
  • Knowledge of GCP regulatory requirements
  • Knowledge of drug product supply requirements
  • Ability to handle multiple tasks with competing priorities
  • Ability to utilize a wide range of computer applications and tools

The pay range that the Company reasonably expects to pay for this headquarters-based position is $129,400 - $152,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Applicants must be currently authorized to work in the United States on a full-time basis.
For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link.
Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.
Please visit our website at: https://www.corcept.com/
Corcept is an Equal Opportunity Employer
Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.

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