TMF Lead (EUROPE - Home based)
IQVIA
Barcelona, Spain
hace 5 días

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment.

The sector we work in is cutting edge with therapies for un-met medical need.

IQVIA Biotech Offers Candidates

  • Intensive Onboarding Programmes
  • Home-based working
  • Regular line manager support and oversight ensuring good work / home life balance for proactive career development
  • Private health insurance
  • 1000’s of online training sessions.
  • Mentorship for all new starters
  • Free eye test
  • ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES :

  • Oversees efforts of site file maintenance and study close out with team members for a designated global project(s)
  • Works with Management to discuss projected hours for the assigned project and provides updates to appropriate project team member(s).
  • Serves as core team member in interactions with the sponsor and sites.
  • Responsible for study specific training and mentor staff as needed.
  • Provide oversight and QC site level documents for the quality and regulatory compliance from maintenance through close out phase.
  • Performs analysis of Quality Metrics reports from the TMF as applicable and escalates concerns to PM / Manager.
  • Manages periodic investigator site file reviews on assigned project(s) to ensure compliance with GCPs and IQVIA Biotech’s standard operating procedures.
  • And communicates findings with MN-R.

  • Ensures the File Review Plan is finalized for each study they oversee
  • Oversees site level timelines. Documents study challenges and communicates them to the department Manager, Sr. Mgr. or Associate Dir. and Project Manager.
  • Assist in collection of the ongoing regulatory documents from sites as necessary.
  • Escalate any site file issues to management as appropriate.
  • Oversees the distribution of updated documents (e.g. 1572, FDF) to client on a monthly basis as required.
  • Ensures necessary IRB / EC documentation (i.e. IRB continuing review, Amendment approval) Site level ICF review, and tracking system updates are completed, as necessary, and as applicable to region.
  • Manages MN-R in ensuring that Investigator names are in the Clinical Trial Management System (CTMS).
  • Updates templates during maintenance phase for regulatory documents specific to local and central Institutional Review Board (IRB) / Ethics Committee (EC) submissions, as applicable per region.
  • Responsible for compiling and distribution of ongoing regulatory documents to sites, as required.
  • Supports the Associates / Specialists on local IRB / EC submissions as necessary and operates as an escalation point of contact for any site / documentation issues.
  • Identifies out of scope activities to Management, Project Manager and team and assures that such activities do not begin until the client provides authorization.
  • Assures that team members understand budgets for the studies they are working on and are accountable for maintaining project activities within documented scope and budget.
  • Oversees any additional duties as outlined in the Site Level TMF plan as applicable.
  • Serve as IQVIA Biotech liaison with Central IRBs
  • Participates in financial and / or resource forecasting
  • Attends internal, external and client audits as applicable.
  • Performs other duties as required.
  • KNOWLEDGE, SKILLS & ABILITIES :

  • Demonstrated ability to lead a team of individuals in the document management process.
  • Extensive knowledge of clinical research process and medical terminology including the submission process
  • Strong written and verbal communication skills to express complex ideas to study personnel, internal and sponsor team members.
  • Excellent organizational and interpersonal skills.
  • Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities.
  • Ability to manage multiple competing priorities within various clinical trials.
  • Extensive knowledge of current ICH GCP guidelines and applicable regulations.
  • Demonstrated knowledge & involvement in audit preparation
  • Ability to gain successful outcomes in areas of challenge regarding the TMF & document management
  • Ability to work independently, prioritize and work with a matrix team environment is essential.
  • Working knowledge of Word, Excel is required.
  • CRITICAL JOB FUNCTIONS :

  • Limited travel may be required
  • Very limited physical effort required to perform normal job duties
  • MINIMUM RECRUITMENT STANDARDS :

  • 5 years of regulatory document management experience
  • Experience in mentoring staff and driving team collaboration is preferred
  • Equivalent combination of education, training and experience
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