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Regional Project Lead

79% Flex
EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE
Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Degree in Life Sciences or equivalent, 4+ years healthcare/clinical experience, Fluency in Spanish and English, Site monitoring + Lead Monitor experience, Proficiency in MS Office applications.

Key responsabilities:

  • Coordinate project team activities
  • Supervise performance of clinical team members
  • Ensure projects compliance with regulations
  • Act as point of contact & collect/report updates
  • Prepare study documents and oversee site visits
PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

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Company Description

PSI is a leading Contract Research Organization with more than 27 years in the industry offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

    Job Description

    Only CVs in English will be considered

    In this position, you will be responsible for coordinating activities of project teams ensuring milestones are met and ensuring consistency of Clinical Operations processes across regions. This function holds project managerial responsibilities under supervision. 

    Responsibilities will include: 

    • Coordinating project team work, supervising the clinical project team members’ performance, 
    • Implementation, and management of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents,
    • Acting as a point of contact for the project team, PSI support services and contractors,
    • Collecting and reporting project status updates,
    • Developing and updating project planning documents, essential study documents and project manuals/ instructions,
    • Conducting and supervising therapeutic area training of the project team and Investigators,
    • Supervising preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits and reviewing site visit reports,
    • Overseeing investigator and site payments,
    • Supervising project team preparation for study audits/inspections and resolution of audit/inspection findings,
    • Coordinating preparation of initial and follow-up Regulatory and Ethics Committee submissions and notifications,
    • Performing other project management tasks in agreement with the responsible Clinical Operations Manager following adequate and documented training, and formal delegation of tasks.

     

     

    Qualifications
    • College/University degree in Life Sciences or an equivalent combination of education, training & experience,
    • Full working proficiency in Spanish and English,
    • At least 4 years’ experience in a health care or clinical environment,
    • Minimum 4 years’ site monitoring experience and at least 2 years’ experience as Lead Monitor or equivalent,
    • Availability to travel,
    • Proficiency in MS Office applications
    • Ability to plan and work in a dynamic team environment
    • Communication, collaboration, and problem-solving skills

    Additional Information

    If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

    Required profile

    Experience

    Level of experience: Mid-level (2-5 years)
    Industry :
    Pharmaceuticals
    Spoken language(s):
    English
    Check out the description to know which languages are mandatory.

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