Job type full-time
Full job description
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., good clinical practice (gcp) and international conference on harmonization (ich) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulationsEscalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (crf) completion and submission, and data query generation and resolutionMay support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the trial master file (tmf) verify that the investigator`s site file (isf) is maintained in accordance with gcp / ich and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Bachelor`s degree degree in scientific discipline or health care preferredReq
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Some organizations require completion of cra training program or prior monitoring experience.
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., good clinical practice (gcp) and international conference on harmonization (ich) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of microsoft word, excel and powerpoint and use of a laptop computer and iphone and ipad (where applicable).
Written and verbal communication skills including good command of english language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Iqvia is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industryWe believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier worldLearn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilitiesHttps://jobs.iqvia.com/eoe
As the covid-19 virus continues to evolve, iqvia’s ability to operate and provide certain services to customers and partners necessitates iqvia and its employees meet specific requirements regarding vaccination statusHttps://jobs.iqvia.com/covid-19-vaccine-status
Posted 2 days ago