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Senior Clinical Project Manager- Oncology

Company

Fortrea
Address , Remote
Employment type FULL_TIME
Salary $105,000 - $182,000 a year
Expires 2023-10-02
Posted at 9 months ago
Job Description
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Senior Project Manager
This position is remote based, anywhere within the US or Canada.

At times working under the direction of a Project Director; the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met. The Senior Project Manager is expected to have a working knowledge of drug development and clinical trial execution. They also compile and drive documentation for the project, ensuring the accuracy and quality of regulatory data.

Operational delivery
  • Accountable for project delivery with regards to agreed time, scope, cost and quality.
  • Team Communication: Serve as key client contact for assigned projects, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business.
  • Serve as escalation point for project issues to internal and external stakeholders, as appropriate.
  • Proactively identify and resolve conflicts as needed
  • Lead core project team(s) and facilitate team's ability to lead extended project team(s), ensuring effective cross-functional teamwork among project team members including both internal and external stakeholders. Depending on size and scope of project(s), this job duty may be performed in collaboration with a Project Director.
  • Quality: Create and manage variance to required project plans. Per SOPs, implement and monitor progress against project plans and revise as necessary. Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs, providing performance feedback to team member’s respective supervisors.
  • Cost: Understand the project delivery strategy, costing assumptions and resulting budget for assigned project(s).
  • Aid in development and maintenance of key project performance indicators for client specified metrics, ensuring that the KPIs are within scope of the project contract.
  • Scope: Deliver project(s) to scope, schedule and costs, ensuring all remain on track with the contract and with financial performance targets. Initiate and implement appropriate actions to proactively manage the change control process both internally and externally.
  • Risk: Proactively lead both quality control and risk assurance activities to ensure project deliverables are met according to regulatory, Fortrea, and client requirements.
  • Define and manage project resource needs and establish succession plans for key resources.
Business Development
  • Perform other duties as assigned by management
  • In collaboration with relevant departments, prepare and deliver presentations for new business as required
Travel: Up to 30% travel required both domestic and international including overnight stays.

Required:
University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.

Preferred:
Master or other advanced degree.
PMP certification.

Minimum Qualifications Required:
  • 4 + years of current experience working as a Project Manager or Senior Project Manager at a CRO managing full-service global trials/studies and the responsibility of the financial management of the studies.
  • Oncology exprience as a Project Manager is required.

On the Job Experience:
  • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
  • Minimum of seven (7) years of relevant clinical research experience in a pharmaceutical company/CRO, including at least two (2) years of full project management responsibility.
  • Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access and Power Point).
  • Experience managing projects in a matrix and virtual environment.
  • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
  • Financial awareness and ability to actively utilize financial tracking systems
  • Demonstrated ability to handle multiple competing priorities and to utilize resources effectively,
  • Excellent communication, planning and organizational skills.
  • Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
  • Ability to work independently and mentor junior project team members.
  • Ability to present to staff at all levels.
  • Ability to negotiate and liaise with clients in a professional manner.
  • Good knowledge of project management processes.

Pay Range: $105,000 - $182,000 USD
Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable. For more detailed information, please
click here
.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our
Privacy Statement
.