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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #02563 Email this job to a friend
About our client
A global CRO that serves the pharmaceutical, biotechnology and medical device industries, our client is built upon a strong foundation of clinical, process and systems expertise. They specialise in major therapeutic areas such as oncology and dermatology. The company has supported more than 51 FDA approvals to date, with no refusals among submissions accepted for filing.
Position Location
Senior Director of International Clinical Project Management Massachusetts
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Direct and coordinate all aspects of US Clinical Operations
2) Provide departmental leadership and direction
3) Develop sponsor contracts and budgets, as well as source personnel
4) Implement and revise standard processes and procedures
5) Oversee budget, timelines and deadlines
6) Ensure efficient and high quality execution of work
7) Support and encourage a multicultural approach and facilitate co-operation between countries and international offices
8) Ensure efficient and high quality execution of work
9) Interact and collaborate with European counterparts and affiliate managers at each location
10) Ensure harmonization of Clinical Operation strategies and delivery of projects globally
11) Oversee resource planning and allocation
12) Direct interviewing and hiring recommendations of new Clinical Operations staff, lead disciplinary actions, deliver performance reviews
13) Co-ordinate resource distribution across projects
14) Direct personnel activities and provide guidance for professional development of staff through active training (operational, scientific)
15) Prepare career development plans, performance reviews, salary actions and work on other administrative tasks
16) Conduct business development activities
17) Respond to requests from business development by actively supporting (or make available the appropriate Clinical Operations staff to actively support) the preparation and defense of proposals
18) Conduct capabilities presentations, consultations, congress attendance and direct client communication
19) Provide strategic direction in assessing relevant new technologies and procedures
20) Review and approve documents, including relevant SOPs
21) Provide recommendation to senior executives for improving and developing the department
22) Participate and assist US and global heads of Clinical Operations in developing corporate strategies and initiatives, departmental management, etc.
23) Ensure attainment of corporate objectives
24) Develop and maintain a sound plan of intra- and inter-departmental relationships
25) Facilitate efficient resource planning and utilization
26) Ensure optimal levels of billability of all staff
27) Identify problems and implement corrective action plans
28) Ensure collation, collection and interpretation of meaningful activity data (metrics) in order to enable accurate awareness of time use
29) Represent the company in relationship with major customers, suppliers, government agencies, etc.
30) Work as backup for managers and directors depending on workload (if needed)
31) Perform all other tasks as assigned
Requirements
1) University degree in Medical or Biological Science (advanced degree preferred) or equivalent combination of education and experience with exposure to quantitative research methodology
2) Minimum 10 years of clinical research experience
3) Minimum 6 years of management experience, including at least 5 years in an international setting
4) Experience as a PM
5) Proven ability to lead teams (preferred)
6) Experience in handling a director level position in an entrepreneurial environment

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