Regulatory Start up Project Manager

Study Start Up Madrid, M


Position at Premier Research

Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases.

We’re looking for an exceptional Regulatory Start up Project Manager to bring your passion to our team. You will be encouraged to grow professionally and personally while enjoying cross-functional partnerships with genuinely supportive colleagues, regardless of location or seniority. Most importantly, you will be using your skills to bring tangible hope to critically ill patients around the world.

At Premier Research, we are science-minded and heart-centered. Join us.

You'll be doing: 

  • Responsible for developing the Regulatory & start-up submission project plan. Is the driver for CA, EC and LEC submission as well other boards/evaluating bodies, import and export licenses, where applicable.
  • Responsible for the pertinent notifications throughout the trial (e.g. First patient-in, End of Trial)
  • Is the liaison with the Sponsor regarding approval and collection of all core documents, country submission packages and commination and adherence to timelines and deliverables
  • Responsible for identifying & communicating country timelines to our clients and project teams
  • Responsible for identifying & communicating risks and contingency plans related to start up activities to our clients and project teams
  • Oversees the site contract execution process in the studies that a Contracts Lead is not assigned
  • Obtains the EudraCT number where delegated by Sponsor
  • Generates and obtains appropriate Sponsor approval for master core documentation e.g. Submission cover letters and EudraCT xml etc.
  • Reviews master IP labels and provides feedback on its potential acceptability to regulatory authorities including issues related to country adaptation
  • Oversees the regulatory approval of IP release
  • Ensures continuous improvement of quality in all Regulatory and Start-up components at the project level (clinical trial applications, essential document collection, communication to Competent Authority and Ethics Committees, etc.).
  • Assumes responsibility on deliverables in Regulatory and Start-up at the project level following the project requirements and the applicable rules
  • Complies with forecasted submission/approval timelines; if forecasted timelines are not reached or if any potential issue is identified, escalates the problem as soon as identified and provides suggestions for resolution
  • Produces and/or reviews submission components like the Patient Information Form/ICF
  • To the level of competence of the RSM, may participate in the review of the Investigational Medicinal Product Dossier (IMPD) in conjunction with other Subject Matter Experts
  • May serve as an Independent Essential Document Reviewer and/or perform second pass review of Essential Documents.
  • Must have direct access to the study budget and must communicate pertinent information related of such budget to the Start-Up staff so that they understand contractual expectations. If there is a significant deviation between the tasks and the contracted budget, the RL must discuss the situation with the PM until confident the discrepancy will be resolved.
  • Attends Kick-Off Meeting, when required
  • At all times to maintain good, friendly and professional relationships with past, current and potential sponsors, and others with whom the company works.

You'll need: 

  • Education to university degree level (pharmacy, medicine or related natural sciences are a plus)
  • Minimum of 5 years professional experience in the clinical research area, in Regulatory and/or Start-up functions at a local/country level, for newly awarded studies containing countries from the same region, and may take a multi-region study in Start-up under supervision, or maintenance studies independently
  • At least 2 years of hands-on experience in the submission of clinical trial applications
  • Working knowledge of FDA Guidance Documents / EU Directives / ISO14155 regulations, drug / device development, and start-up procedures
  • Knowledge of ICH / GCP regulations / country specific regulations as applicable
  • Ability to work accurately and to interpret the relevant directives and guidelines
  • Working knowledge of professionally recognized tools for planning and management of scope, timeline, resources, and budget