The Senior Project Manager leads and manages multiple complex projects, interfaces with various departments and stakeholders, and ensures effective execution of clinical development initiatives. This role requires strong project management skills, with an emphasis on clinical research and communication.
Job Description:
Senior Project Manager
The Senior Project Manager provides management and leadership to plan, prepare, and execute multiple complex and high profile projects. Internally, the Senior Project Manager interfaces with clinical monitoring and site management, clinical data management, SAS programming, biostatistics, pharmacovigilance, and medical writing. S/he also interfaces internally with business development, corporate compliance and company leadership, and externally with sponsors and external vendors.
What we do
For more than 30 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 $130-150K USD plus applicable bonus. This hiring range is specific to 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.
- 6 to 8 years of relevant clinical research experience in a Clinical Research Organization/Pharmaceutical Company, with a minimum of 3 years of Project Management experience in a CRO or pharmaceutical company required. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case by case basis.
- 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.
- Excellent clinical trial project management, written and oral communication, organizational, and interpersonal skills are required.
- Proficiency in English (written and verbal).
- Action-oriented and resilient in a fast-paced environment and will have the ability to build and lead effective project teams, motivate others, delegate, and make and implement decisions.
- 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.
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Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Top Skills
Biostatistics
Clinical Research
Communication Skills
Medical Writing
Organizational Skills
Pharmacovigilance
Project Management
Sas Programming
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