Description: The Judge Group has a new opportunity for a Sr Clinical Scientist. We are looking for a Senior Clinical Scientist contractor to support the maintenance of marketed products. Key responsibilities include regulatory filings, regulatory correspondence, and report preparation. Candidates should have 3-5 years of drug development experience, with a preference for those experienced in developing products for bleeding disorders.
The role involves guiding a multi-disciplinary, multi-regional, matrix team through complex decisions, integrating input from various disciplines to create, maintain, and execute global plans for product maintenance and geographic expansion.
Key Responsibilities:
Leadership:
Demonstrate a global perspective and ability to work across functions, regions, and cultures.
Identify challenges and opportunities, making informed recommendations.
Collaborate effectively to build credibility and confidence within and outside the company.
Promote diversity and inclusion, modeling these behaviors for the organization.
Invest in the development and success of others.
Decision-Making and Autonomy:
Make decisive and sound judgments with limited information.
Present clear business arguments and strategic recommendations using both quantitative and qualitative evidence.
Balance input from multiple stakeholders to drive solutions and set priorities.
Incorporate feedback and ensure swift decision-making for flawless execution.
Develop executable plans, meeting budget and deadlines.
Interaction:
Utilize organizational savvy to align and execute effectively within and outside the BU.
Recognize the importance of connections and engage key stakeholders for optimal solutions.
Communicate persuasively, both verbally and in writing.
Exhibit exceptional communication, negotiation, presentation, and influencing skills across stakeholders.
Complexity:
Deliver solutions to abstract problems across functional areas.
Identify and solve fundamental issues through assessment of intangible variables.
Recommend key decisions, escalate issues as needed, and persuade stakeholders with exceptional influencing skills.
Create clarity of accountabilities in a global, highly matrixed organization.
Requirements:
3-5 years of experience in clinical research drug development within the pharmaceutical or biotech industry.
