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Executive Director Of Consulting (Us Or Europe)
Company | Catalyst Clinical Research |
Address | Raleigh, NC, United States |
Employment type | FULL_TIME |
Salary | |
Category | Internet Publishing |
Expires | 2023-10-06 |
Posted at | 7 months ago |
Catalyst Clinical Research is a niche provider of clinical research services through two established solutions- Catalyst Flex and Catalyst Oncology. Here at Catalyst Clinical Research we provide support and services exclusively to biotech companies because we know and understand the biotech environment. Our 15+ years of experience allow us to quickly grasp the evolving needs of our clients so we can deliver the solutions essential to meet the evolving needs and unexpected changes inherent in oncology development. When protocols amend or emerging data suggest a breakthrough straight from Phase I to registration, we are ready.
- Responsibility for consulting business operational delivery.
- Represent company at conferences, client meetings, functions.
- Assisting with the management and reporting of all department financial and operational metrics.
- Oversight of consulting contracts. responsible for overseeing/liaising with the administrative support team (i.e., Consulting Proposals, Consultant Contracts, Finance, general admin).
- Perform other duties as assigned.
- Identify and manage initiatives to drive department growth and success.
- Manage and assure sponsor expectations are met or exceeded.
- Oversee the production of reports or outputs from the consulting effort and drive the timelines and budget management process to ensure timely and appropriate output.
- Ensure staff training is up to date.
- Responsible for managing and delivering to the business targets and liaising with consultant pool from a planning perspective to establish client team composition and drive recruitment of new consultants/employees through department heads and people ops organization.
- Manage all resources.
- A minimum of 5 years line management experience.
- A minimum of 15 years of relevant work experience.
- A satisfactory combination of education and experience may be accepted as a substitute for the specific education and experience listed above.
- Regulatory experience is highly preferred.
- Can attend study team meetings as needed.
- Ability to diffuse high stress situations in a professional manner.
- Ability to work independently and as a member of various teams and committees.
- Good judgement with the ability to make timely and sound decisions.
- Able to work independently on multiple, concurrent projects.
- Versatility, flexibility, and a willingness to work within constantly changing priorities.
- Extensive knowledge of clinical trial study design.
- Creative, flexible, and innovative team player.
- Excellent verbal, written, and interpersonal skills.
- Proficient with Microsoft Office Suite.
- Comfortable with being client-facing.
- A high degree of accuracy and attention to detail.
- Commitment to excellence and high standards.
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