Senior Transparency Specialist

Summary

Join MMS, an award-winning, data-focused CRO, and become a Senior Transparency Specialist. We offer a supportive and innovative work environment with a global footprint. In this role, you will provide operational support for clinical trial transparency, data sharing, and document redaction. You will be responsible for high-quality deliverables, regulatory compliance, and project leadership. MMS is known for its exceptional culture and industry-leading employee retention. Discover more about our exciting opportunities and why MMS is a great place to advance your career.

Requirements

• Bachelor’s Degree in a scientific, medical, or clinical discipline or related field is preferred; or 5 years of experience if less than a Bachelor’s
• At least 4 years of previous transparency experience
• Effective problem-solving and data analysis skills
• Has a strong attention to detail

Responsibilities

• Responsible for providing high-quality transparency deliverables in an efficient manner
• Technical expertise on regulatory requirements (EMA Policy 0070, HC PRCI, EU-CTIS etc.)
• Facilitates the initiation, progression and completion of the exchange of information for all Transparency workflow steps, with skill and proficiency
• Performs quality control reviews of document redaction or anonymization to ensure consistency and accuracy
• Maintain a strong understanding of regulations and guidance’s as they pertain to transparency; ensure deliverable timelines are compliant with regulatory timelines
• Lead projects with minimal management oversight, including complex projects with multiple team members; coordination independently with the client
• Tailors communication to diverse audience considering experience, background, and expectations
• Anticipate and understand customer’s needs and preferences and can provide solutions to customer’s needs; Develops deliverables according to customer specifications
• Effectively manage/ prioritize multiple deliverables and delegate as needed or implement workable solutions to complete deliverables on time
• Capable of leading Transparency process/tools improvements initiatives and may participate in complex companywide process improvement initiatives
• Facilitates and fosters positive team environment while supporting independent action to achieve team goals

Preferred Qualifications

• Hands-on experience with clinical trials and pharmaceutical development
• Experience in the pharmaceutical or CRO industry