Senior Project Manager

Posted 11 Days Ago
Be an Early Applicant
England
Senior level
Other
The Role
The Senior Project Manager oversees and ensures the successful execution of complex clinical research projects, collaborating with various internal teams and external stakeholders. Responsibilities include managing relationships, maintaining compliance with regulations, and leading project teams effectively while delivering results in a fast-paced environment.
Summary Generated by Built In

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 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 £45-65K plus applicable bonus. This hiring range is specific to UK 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.

#LI-SS1

Driving/Travel requirements - Travel up to 25% (US, Canada, or International)

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.

Top Skills

SAS
The Company
Basel
443 Employees
On-site Workplace

What We Do

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.​

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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 [email protected]. Be vigilant

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