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Mms Holdings Jobs (NOW HIRING)

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and ...

McKesson

Sr. Counsel - Litigation & Investigations

Atlanta, GA · On-site +1

$134K - $182K/yr

The Role: The MMS Legal Department is seeking a Senior Counsel to join its Technology, Risk ... Select and manage outside counsel, including setting scope, controlling cost, and holding firms ...

McKesson

Sr. Counsel - Litigation & Investigations

Atlanta, GA · On-site +1

$134K - $182K/yr

The Role: The MMS Legal Department is seeking a Senior Counsel to join its Technology, Risk ... Select and manage outside counsel, including setting scope, controlling cost, and holding firms ...

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Mms Holdings information

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$32K

$136.5K

$217K

How much do mms holdings jobs pay per year?

As of Aug 7, 2026, the average yearly pay for mms holdings in the United States is $136,471.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,000.00 and $150,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical data manager at MMS Holdings, and why are they important?

A Clinical Data Manager at MMS Holdings typically requires a solid background in life sciences or related fields, experience in data management, and familiarity with clinical trial processes. Proficiency in electronic data capture (EDC) systems, CDISC standards, and clinical data management software, along with relevant certifications like CCDM, is highly valued. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These skills ensure high-quality, compliant data management that supports successful clinical trial outcomes and regulatory submissions.

What types of projects and clients does an employee typically work with at MMS Holdings, and how does this impact daily responsibilities?

At MMS Holdings, employees often collaborate with a diverse range of clients, including pharmaceutical, biotech, and medical device companies, on projects such as clinical trial data management, statistical programming, and regulatory submissions. This variety means daily responsibilities can shift between data analysis, report writing, and cross-functional meetings with both internal teams and client representatives. Project assignments often require adapting to different therapeutic areas and regulatory standards, which fosters continuous learning and professional growth. Teamwork is emphasized, with frequent opportunities to collaborate with statisticians, medical writers, and project managers.

What is the difference between Mms Holdings vs Clinical Data Coordinator?

AspectMms HoldingsClinical Data Coordinator
Required CredentialsBachelor's in Life Sciences or related field; relevant certificationsBachelor's in Life Sciences or related field; data management certifications preferred
Work EnvironmentPharmaceutical research, clinical trial support, office settingClinical trial sites, hospitals, research organizations
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, pharmaceutical companies

Both roles involve handling clinical data, but Mms Holdings typically focuses on data management within pharmaceutical research companies, while Clinical Data Coordinators often work directly at clinical trial sites or hospitals. The roles share similar credentials but differ mainly in work environment and specific responsibilities.

What does MMS Holdings do?

MMS Holdings is a global contract research organization (CRO) that provides a range of services for the pharmaceutical, biotech, and medical device industries. Their offerings include clinical trial management, data management, biostatistics, regulatory submissions, medical writing, and pharmacovigilance. MMS Holdings helps sponsors bring their products to market by supporting drug development from early phases through post-marketing. The company is known for its scientific expertise, data-driven approach, and commitment to quality in regulatory submissions.
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Mms Holdings jobs near you
Infographic showing various Mms Holdings job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $136,471 per year, or $65.6 per hour.

Senior Medical Writer (Remote - US)

MMS Holdings Inc.

Remote

Full-time

Re-posted 19 days ago

Job description

About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions - rooted in strong science and decades of regulatory experience - that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
  • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator's brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • Mentor medical writers and other members of the project team who are involved in the writing process

Requirements
  • At least 3 years of previous experience in the pharmaceutical industry
  • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
  • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • Exceptional writing skills are a must
  • Excellent organizational skills and the ability to multi-task are essential prerequisites
  • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
  • Experience being a project lead, or managing a project team
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

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