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Senior Manager, Clinical Trial Transparency

Baltimore, MD
  • Posted: over a month ago
  • Full-Time
Job Description

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. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO in Global Health & Pharma’s international awards programs for the last three consecutive years. For more information, visit or follow MMS on LinkedIn.


  • Provide leadership, mentorship, and develops personnel by maintaining a positive work environment while overseeing the daily activities of personnel.
  • Strong expertise in transparency services including clinical trial disclosures, redaction and anonymization and patient communications.
  • Interacts directly and independently with client to coordinate all facets of the project; expert communicator who has developed strong relationships with client.
  • Makes decisions and advises others on complex problems; understands intra- and inter-departmental implications of decisions and can develop strategic solutions with minimal input.
  • Responsible for overseeing and ensuring high-quality transparency deliverables in an efficient manner including document redaction and anonymization.
  • Effectively communicates with team/functional leadership, and members of senior management.
  • Oversees and leads the initiation, progression, and completion of the exchange of information for all Transparency workflow steps, with high skill and proficiency.
  • Strong project management knowledge, including managing complex projects with multiple team members requiring independent coordination with the client.
  • Leads and participates in business development activities.
  • Proactively identifies areas for improvement before issues arise and provides strategic proposal/resolution for consideration.
  • Capable of leading Transparency process/ tool improvement initiatives and may participate in complex companywide process improvement initiatives.
  • Knowledge on using anonymization tools with quantitative risk assessment.
  • Develops and maintains SOPs, work practices, forms and other documentation, and training materials related to clinical trial disclosures and transparency services.
  • Maintains a strong understanding of regulations and guidances as they pertain to transparency; and ensures alignment with company systems and working practices.
  • Identifies new industry trends relevant to trial transparency including impacts of changing regulations in this area and impacts to other departments.

Job Requirements: 

  • Graduate degree in scientific, medical, clinical discipline or related field, or related experience.
  • At least 5 years of experience in a CRO environment.
  • Demonstrates managerial skills and prior management experience preferred.
  • Sound understanding of clinical development and operations implementation and management, the drug development process, and regulatory guidelines.
  • Excellent Scientific Writing Skills.
  • Excellent analytical, organizational, and problem-solving skills.
  • Proficiency with MS Office Applications.
  • Strong communication and presentation skills required.
  • Familiarity with ISO 9001:2015 and ISO 27001:2013 standards preferred.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific and clinical data/ terminology, and the drug development process.

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Baltimore, MD



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