Senior Budget and Contract Analyst (home-based)

Hobson prior are seeking a Senior Budget and Contract Analyst to join a global medical devices company who are committed to transform people's lives through new medical solutions that can improve the health of patients worldwide. This is a home-based position either in Paris, Munich, or Madrid.

Please note that to be considered for this role you must have the right to work in this location.

Job Responsibilities:

• To work self-sufficiently and proactively to coordinate all necessary contract and budget activities during study start-up.
• Manage large portfolio of contract and budget related activities across several studies and division portfolios.
• Coordinate with leadership and clinical study teams to continually prioritize contract and budget reviews as new information and/or considerations are introduced to keep pace with the overall service level targets.
• Provide updates to the leadership on site start up activities, investigator readiness, regulatory submission and approval status, etc.
• Develop and foster clinical research site relationships to become a subject matter expert in the contracting and budget finalization process for select clinical research sites.
• Maintain and stay current with divisional clinical study team priorities as applicable to active contracting and budget finalization timelines.
• Ability to facilitate CSA and budget negotiations with clinical research site.
• Engage management and clinical study teams consistent with escalation pathways, including the identification of risks that may impact achievement of service level agreements and/or study goals.
• Develop, prepare, complete and track required contracting, budget and legal documentation.
• Update and maintain study-specific start-up trackers as it relates to contracting and budget details.
• Any other assigned duties.

Key Skills:

• Ability to multi-task: support several studies and/or personnel simultaneously, work in a very fast-paced environment.
• You are comfortable interacting with clinical research site personnel via phone, email, and in person.

Requirements:

• Bachelor's Degree, or an equivalent combination of experience and education.
• At least 4+ years' experience in clinical/scientific research and medical device experience.
• Previous experience working with clinical research centers.
• Previous experience working with clinical trial management systems (e.g. Siebel CTMS, Veeva) and clinical document control systems / eTrial Master Files.
• Previous experience following standard operating procedures and work instructions in a quality environment.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.