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Merck Contract Jobs (NOW HIRING)

Merck

Documentation Specialist

Durham, NC · On-site

$20 - $25/hr

... contract position. This onsite role is critical for maintaining compliance and site inspection ... Merck discovers, develops, manufactures, and markets a broad range of innovative products to ...

New

BCforward

Desktop Support

Billerica, MA

$17.86/hr

CE 5 (possible contract to hire) End Client: Merck Minimum Wage to Contractor: $17.86 Job Duties: Responsible for installing, maintaining and repairing company and multi-vendor systems which include ...

LanceSoft Inc

Supplier Quality Manager

Athens, GA

... a contract, contract to hire, or permanent hire basis. Our Clientele: Johnson & Johnson, Merck, Pfizer, Novartis, Purdue, Eisai, Aetna, Becton & Dickinson, Actavis Pharmaceutical, Shire ...

LanceSoft Inc

Quality Engineer III

North Haven, CT

$71K - $92K/yr

... a contract, contract to hire, or permanent hire basis. Our Clientele: Johnson & Johnson, Merck, Pfizer, Novartis, Purdue, Eisai, Aetna, Becton & Dickinson, Actavis Pharmaceutical, Shire ...

Infosys

Line Partner - SAP - Life Sciences

San Francisco, CA · On-site

$422K - $615K/yr

Along with a team of consulting leaders, drive sales pursuits and manage contract negotiations for ... Merck, Organon, Zoetis, Alcon, Bausch & Lomb, Boston Scientific, Medtronic, Smith & Nephew, Viatris ...

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Merck Contract information

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$60.5K

$99.5K

How much do merck contract jobs pay per year?

As of Jun 26, 2026, the average yearly pay for merck contract in the United States is $97,205.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a Merck Contract role, and why are they important?

To thrive in a Merck Contract position, you typically need expertise relevant to the pharmaceutical or life sciences industry, such as a background in biology, chemistry, or business, along with experience in contract management or procurement. Familiarity with contract management systems, regulatory compliance tools, and proficiency in software like SAP or Oracle are often required. Strong negotiation, attention to detail, and effective communication are crucial soft skills for managing agreements and collaborating with stakeholders. These competencies help ensure that contracts are compliant, cost-effective, and aligned with organizational goals.

What types of projects can I expect to work on as a contractor at Merck, and how does this differ from full-time roles?

As a contractor at Merck, you will typically be assigned to project-based work in areas such as research and development, clinical trials, regulatory affairs, or IT systems, depending on your expertise. Contractors often focus on specific deliverables within a defined timeframe and may work alongside full-time employees in cross-functional teams. While you will benefit from Merck's collaborative environment, contractors usually have less involvement in long-term strategic planning or company-wide initiatives compared to permanent staff. This project-based structure offers exposure to diverse challenges and can help expand your professional network within the pharmaceutical industry.

What is a Merck contract?

A Merck contract refers to a formal agreement between Merck, a global pharmaceutical company, and another party such as a supplier, healthcare provider, research organization, or distributor. These contracts outline terms for the supply of products, research collaborations, licensing, or distribution of pharmaceuticals. The agreements ensure compliance with regulations, define responsibilities, and protect the interests of both parties. Merck contracts typically include clauses on confidentiality, intellectual property, dispute resolution, and pricing. Understanding the specifics of a Merck contract is crucial for successful partnerships and regulatory compliance.

What is the difference between Merck Contract vs Merck Clinical Research Associate?

AspectMerck ContractMerck Clinical Research Associate
Required CredentialsTypically requires a bachelor's degree in life sciences or related field, with some roles needing clinical research certificationsRequires a bachelor's degree in life sciences, healthcare, or related field; certifications like CCR or ACRP are common
Work EnvironmentContract-based roles within pharmaceutical or biotech companies, often in office or clinical settingsWorks in clinical trial sites, hospitals, or research facilities, often traveling between sites
Employer & Industry UsageUsed by pharmaceutical companies like Merck for temporary or project-based staffingCommonly employed by pharmaceutical companies, CROs, or research institutions for clinical trial monitoring

In summary, Merck Contract roles are typically temporary positions within the company, focusing on specific projects, while Merck Clinical Research Associates are responsible for monitoring clinical trials, often working at trial sites. Both roles require similar educational backgrounds and certifications, but differ mainly in work setting and job scope.

What cities are hiring for Merck Contract jobs? Cities with the most Merck Contract job openings:
What are the most commonly searched types of Merck jobs? The most popular types of Merck jobs are:
What states have the most Merck Contract jobs? States with the most job openings for Merck Contract jobs include:
Merck Contract jobs near you
Documentation Specialist

Documentation Specialist

Merck

Durham, NC • On-site

$20 - $25/hr

Contractor

Medical, Dental, Vision

This job post has expired today. Applications are no longer accepted.

Merck rating

7.8

Company rating: 7.8 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

43rd of 73 rated pharmaceutical

Job description

We are seeking a detail-oriented professional for a Quality Systems Documentation Management contract position. This onsite role is critical for maintaining compliance and site inspection readiness through the rigorous management of physical and electronic documentation. Working closely with system owners and the broader team, you will ensure total alignment with Good Documentation Practices (GDP) and global and site-specific quality procedures.

Responsibilities

  • Manage document issuance and reconciliation tasks using Veeva, an electronic document management system.
  • Provide archiving assistance for paper records in the High Density Storage Room (HDSR).
  • Partner with system owners to actively maintain the site in an inspection-ready state.
  • Update the Record Inventory Management System (PRIMS) for archived paper documents, including archiving files and fulfilling document check-out requests.
  • Assist the team with organizing paper batch records extracted from SAP to prepare them for issuance.
  • Maintain strict adherence to Good Documentation Practices (GDP) when performing data entry into quality systems.
  • Guide and advise others on proper Quality System procedures and processes to ensure all internal documentation requests are submitted appropriately.

Education

  • A Bachelor's degree is preferred.
  • An Associate's Degree (AA) or a High School Diploma will be accepted if accompanied by at least two years of related GMP Biopharma experience.

Experience

  • Prior experience working within a Good Manufacturing Practice (GMP) environment.
  • Hands-on knowledge or familiarity with an electronic document management system, specifically Veeva.
  • Practical knowledge of a quality system used for documentation, as well as archiving or organizing physical paperwork.
  • Strong computer skills with a focus on data entry proficiency.

Company Description

Merck Sharp & Dohme Corp. ("Merck") is a leading research-driven pharmaceutical products and services company. Merck discovers, develops, manufactures, and markets a broad range of innovative products to improve human health, directly and through its joint ventures
Imagine getting up in the morning for a job as important as saving and improving lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery or scientific genius to work in collaboration with other like-minded colleagues to pursue and bring hope to countless people who are battling the most challenging diseases of our time. Our team is always evolving, so if you are among the intellectually curious, join us—and start making your impact today.

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