We are seeking an experienced 𝗣𝗿𝗶𝗻𝗰𝗶𝗽𝗮𝗹 𝗦𝘁𝗮𝘁𝗶𝘀𝘁𝗶𝗰𝗮𝗹 𝗣𝗿𝗼𝗴𝗿𝗮𝗺𝗺𝗲𝗿 to support global clinical development programs across pharmaceutical, biotechnology, and medical device clients.
The ideal candidate will bring strong expertise in 𝗢𝗻𝗰𝗼𝗹𝗼𝗴𝘆, regulatory reporting, and clinical data standards, with the ability to provide technical leadership while remaining hands-on in the development and delivery of high-quality programming outputs.

• Strong hands-on experience in 𝗦𝗔𝗦 𝗣𝗿𝗼𝗴𝗿𝗮𝗺𝗺𝗶𝗻𝗴 within clinical trials• Strong experience in 𝗢𝗻𝗰𝗼𝗹𝗼𝗴𝘆 clinical trials and therapeutic area-specific reporting• Advanced expertise in 𝗖𝗗𝗜𝗦𝗖 standards, including 𝗔𝗗𝗮𝗠 development and validation• Extensive experience with 𝗧𝗟𝗚𝘀, statistical reporting, data visualization, and graphical outputs• Strong stakeholder management, communication, and cross-functional collaboration skills• Ability to work independently and drive deliverables in a fast-paced environment• Flexibility to work primarily in 𝗨𝗦 𝗣𝗮𝗰𝗶𝗳𝗶𝗰 𝗧𝗶𝗺𝗲 (𝗖𝗮𝗹𝗶𝗳𝗼𝗿𝗻𝗶𝗮) with a few overlapping hours in 𝗜𝗦𝗧 to support global collaboration and project delivery