Project Manager - SRG - new job in Houston, US

Project Manager - SRG
  • Competitive
  • Permanent
  • Houston TX, US Houston HARRIS US 77001
Job Ref: JO000133891
Sector: Clinical
Sub-sector: Project Management
Date Added: 31 October 2022

Job Title: Clinical Trial Project Managers

Job Type: Permanent Full-Time

SRG is a Global Life Sciences staffing and consulting firm is currently seeking several Clinical Trial Project Managers for permanent full-time employment opportunities across the United States (on-site and hybrid). At SRG, we are taking STEM careers further because we are the leader in the Life Science human capital industry and are hiring for science, clinical and engineering jobs to help you develop your scientific career in the right direction. At SRG, we speak your language!

The successful candidate have responsibility for all study management aspects of assigned studies within agreed upon budget, timelines, and internal and external requirements, from study start up to study close out/reporting/filing.

Responsibilities and Key Activities (not limited to):

  • Lead and coordinate the execution of one or more clinical studies from study start-up through data reporting, and inspection readiness to ensure timely delivery of quality study data within agreed upon budget and timelines
  • Ensure that all aspects of clinical research protocols are properly planned and executed according to regulatory requirements (e.g. ICH, GCP) and provide recommendations regarding the operational feasibility of selected study designs
  • Provides leadership to the teams in the setting of realistic recruitment targets and delivery milestones
  • Forecast and manage the Clinical Trial Budget for the program.
  • Identify sourcing strategy for the study and lead Clinical Research Organizations (CRO) selection.
  • Oversees CRO and timeliness/quality of CRO deliverables according to protocol requirements, study plans, health authority regulations, internal Policies/SOPs and ICH/GCP guidelines
  • Oversee drug supply management, flow of drug supply to the sites and spot check of drug accountability at both study and site level.
  • Evaluate study progress reports and results for overall compliance and recommends corrective action, including study termination for non-performance.

Skills and Qualifications:

Education: BS, MS, PhD in relevant scientific and/or biomedical field

  • Minimum 5 Years of clinical research related experience, e.g., as a Clinical Development (or Clinical Trials) manager, preferably in the field of CNS, psychiatry/psychology, or addiction.
    • Previous experience must be in Life Sciences, i.e. Pharmaceutical, Biotechnology or Medical Devices
  • Extensive global clinical trial/study management experience
  • Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations
  • Demonstrated study/project management & leading teams in a matrix environment
  • Demonstrated oversight of CROs; understands how to work with vendors to accomplish tasks
  • Demonstrated experience in managing per subject costs, vendor, ancillary, and monitoring costs projections and spend
  • Ability to interpret study level data, translate and identify risks
  • Ability to proactively identify and mitigate risks around site level in study execution

We thank all applicants in advance for their applications! Please note, only candidates who are selected to be moved forward in the recruitment process will be contacted by a member of the SRG Recruitment Team!

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

26/12/2022 12:00:00
USD 0.00 0.00 Hour
Contact Consultant:
Krista Brenner

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