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Contract Drug Safety Associate Jobs (NOW HIRING)

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Drug Safety Associate

Parsippany, NJ · On-site

Drug Safety Associate Duration: 12 months contract, extendable up to 36 months Location: Parsippany, NJ Note: The client has the right-to-hire you as a permanent employee at any time during or after ...

Viking Therapeutics

Drug Safety Associate

San Diego, CA · On-site

$77K - $90K/yr

The Drug Safety Associate provides operational and documentation support for the company's clinical safety and pharmacovigilance activities. Working closely with the Drug Safety Manager, this role ...

OSI Pharmaceuticals

Drug Safety Associate

Boulder, CO · On-site

The Safety Associate works fairly independently in receiving and reviewing serious adverse event (SAE) reports for completeness, performing initial triage, data entry into the Safety database and ...

Integrated Resources INC

Drug Safety

Horsham, PA

Standard Operating Procedures and Working Practices Department guidance documents MedDRA coding dictionary and MedDRA points to consider Understand relevant safety implications regarding contracts ...

Belcan

Drug Safety Coordinator

Clayton, NC · On-site

$19.23 - $26/hr

Requirements: * Associate degree * 2-3 years of recent experience in a clinical setting or ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...

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Contract Drug Safety Associate information

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$12

$49

$85

How much do contract drug safety associate jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for contract drug safety associate in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What does a contract drug safety associate do?

A Contract Drug Safety Associate is responsible for monitoring, collecting, and analyzing information about the safety of pharmaceutical products. They work on a contractual basis, often for pharmaceutical companies or clinical research organizations, to ensure that adverse events and potential side effects are properly documented and reported to regulatory authorities. Their duties may include data entry, case processing, regulatory reporting, and supporting safety audits. These professionals help ensure patient safety and compliance with regulatory requirements throughout the drug development and post-marketing process.

What are the key skills and qualifications needed to thrive as a contract drug safety associate, and why are they important?

To thrive as a Contract Drug Safety Associate, you need a solid understanding of pharmacovigilance principles, adverse event reporting, and experience with regulatory guidelines, often supported by a degree in life sciences or pharmacy. Familiarity with drug safety databases (such as Argus or ARISg), MedDRA coding, and compliance with FDA and EMA regulations is typically required. Strong attention to detail, effective communication, and the ability to manage time-sensitive tasks are crucial soft skills in this role. These competencies ensure accurate safety data management, regulatory compliance, and the protection of patient well-being.

What are some common challenges faced by contract drug safety associates, and how can they be addressed?

Contract Drug Safety Associates often face challenges such as adapting quickly to new company protocols, managing high volumes of case processing within tight timelines, and staying updated with evolving regulatory requirements. Since contract roles may involve working with multiple teams or transitioning between projects, strong communication skills and adaptability are essential. Proactively seeking clarification, utilizing available training resources, and maintaining organized documentation can help overcome these challenges and ensure high-quality work in this fast-paced environment.

What is the difference between Contract Drug Safety Associate vs Contract Pharmacovigilance Associate?

AspectContract Drug Safety AssociateContract Pharmacovigilance Associate
CertificationsTypically requires life sciences or healthcare-related certificationsSimilar certifications, often including pharmacovigilance training
Work EnvironmentPharmaceutical companies, CROs, or biotech firmsSame as Drug Safety Associate, often in clinical or regulatory settings
Industry UsageUsed in drug safety monitoring and adverse event reportingUsed in drug safety, risk management, and regulatory compliance
Job FocusMonitoring adverse events, data entry, case processingMonitoring, reporting, and risk assessment of drug safety data

The Contract Drug Safety Associate and Contract Pharmacovigilance Associate roles are closely related, both focusing on drug safety and adverse event management within pharmaceutical and biotech industries. The main difference lies in terminology used by employers, but their responsibilities, work environment, and required certifications are very similar.

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Contract Drug Safety Associate jobs near you
Infographic showing various Contract Drug Safety Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, 1% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Drug Safety Associate

Peapack, NJ

Global Channel Management, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Global Channel Management, Inc.external

$21/hr

Contractor

Re-posted yesterday

Job description

Company Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. 


Qualifications

Drug Safety Associate  needs 2 years experience.


Drug Safety Associate  requires:

  • management of relational databases
  • Basic understanding of Pharmacovigilance


Drug Safety Associate duties are:

  • Ability to solve routine problems and to surface issues constructively
  • Ability to make basic decisions with an understanding of the consequences
  • Ability to achieve personal objectives while meeting departmental standards of performance
  • Ability to work under supervision in a matrix organization
  • Fluency in spoken and written English


Additional Information

$21/hr

12 months+

Global Channel Management logo

About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

Year founded

2009

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