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Senior Project Manager

Role overview

Qualifications

  • Bachelor’s degree in life/health sciences or related discipline
  • 5 to 8 years of Project Management experience leading global/complex clinical trials in a Clinical Research Organization/Pharmaceutical Company
  • Good working knowledge of drug development process and regulatory requirements
  • Proficiency in English (written and verbal)

Responsibilities

  • Provide management and leadership to plan, prepare, and execute complex clinical trial or regulatory projects
  • Interface with internal departments and company leadership, and externally with sponsors and vendors
  • Lead high performing cross functional project teams and motivate others
  • Build and manage relationships with internal and external team members

Key facts

Other skills

  • Social Skills
  • Planning
  • Organizational Skills
  • Decision Making
  • Problem Solving
  • Mentorship
  • Communication
  • Teamwork
  • Leadership
  • Self-Motivation
  • Resilience

About the company

Veristat logo

Veristat

Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. ​ With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat.​ - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at talentacquisition@veristat.com. Be vigilant.

Company details

Company size501 - 1000

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Job description

Job Description:

Senior Project Manager  

The Senior Project Manager provides management and leadership to plan, prepare, and execute complex and high - profile clinical trial or Regulatory projects and/or programs. They interface with internal departments and company leadership, and externally with sponsors and vendors.  

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat

  • 480+ oncology projects in the past 5 years

  • 350+ rare disease projects delivered in the past 5 years

  • Flexible, inclusive culture — 70% remote workforce, 66% women-led teams

  • Learn more about our core values here!

What we offer:

The estimated hiring range for this role is $130K-150K plus applicable bonus. This hiring range is specific to the USA 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.  

  •  5 to 8 years of Project Management experience leading global/complex clinical trials in a Clinical Research Organization/Pharmaceutical Company Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis. 

  • Executive level communication, written oral communication, interpersonal skills, as well as strong planning and organizational ability are required. 

  • Good working knowledge of drug development process and regulatory requirements, including familiarity with International Conference on Harmonisation (ICH) guidelines and other applicable regulatory rules and guidelines. 

  • Proficiency in English (written and verbal).  

  • Action-oriented and resilient in a fast-paced environment and will have the ability to lead high performing cross functional project teams, motivate others, delegate, including advanced stakeholder communication/ escalation problem solving and decision-making skills.  

  • Ability to build, manage relationships with internal and external team members (vendors, clients etc.) and drive activities to conclusion with minimal support. 

  • 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.

#LI-SI1

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

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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