Senior Manager, Project Management

Job Description

Senior Manager, Project Management

Working under the direction of the department head, the Senior Manager, Project Management is responsible for all project management aspects of projects for clients and project teams, through the successful management of internal staff. S/he plays an active role in the maintenance of optimal department processes, implements effective project-specific strategies, and assists with the development and implementation of department strategies to increase productivity and quality, while decreasing cycle times and costs. The Senior Manager, Project Management also provides business management support to the department head.

Internally, the Senior Manager, Project Management interfaces with project leads and Department Leadership from all functional areas. S/he also interfaces externally with sponsors and external vendors.

What We Do

For more than 27 years, Veristat has built a reputation as global experts in clinical development.

• 760+ Rare Disease Clinical Trials supported
• 160+ Marketing Applications supported
• In 2022 we supported 8 marketing application that received regulatory approval
• Learn more about our core values here!
  
  

What We Offer

• The estimated hiring range for this role is $130,500 - $ 176,000 plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
• Benefits vary by location and may include:
• Remote working
• Flexible time off
• Paid holidays
• Medical insurance
• Tuition reimbursement
• Retirement plans
  

What We Look For

• Bachelor’s degree in life/health sciences or related discipline, or equivalent required.
• 8 years of Project Management experience in a CRO/Pharmaceutical Company, with at least 3-5 years of supervisory experience.
• Familiarity with International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
• Expert knowledge of drug development process and clinical research methods.
• Strong experience in management of study budgets and change order management.
• Demonstrated knowledge of a metrics driven project management approach.
• Demonstrated ability to thoughtfully solve problems, exercise sound judgment, lead by example, and influence without authority.
• Demonstrated ability to think “big picture” and strategically leverage expertise, to serve as a consultant and business partner with internal and external customers.
• Excellent clinical trial project management, written and oral communication, organizational, and interpersonal skills are required.
• Good working knowledge of drug development process and clinical research methods.
• Proficiency in English.
• Action-oriented and resilient in a fast-paced environment and will have the ability to build effective project teams, motivate others, delegate, and make and implement decisions.
• Proficiency in English (written and verbal).
• Ability to build and maintain trust and confidence and communicate effectively with client, external vendors, and internal team members.
• Ability to mentor and delegate.
  
  

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.