Iqvia
Healthcare
ClinicalResearchAssociate2
Neural analysis suggests this role is
optimal for Mid candidates.
“Clinical Research Associate 2 at Iqvia. Skills: Site monitoring, Protocol knowledge, Regulatory compliance. Perform site selection visits. Perform site initiation visits”
Industry & Context.
Problem-solving
What They're Looking For.
Must Have
2-4 years independent on-site monitoring experience, Bachelor's degree in health care or scientific discipline or educational equivalent, In depth knowledge and skill in applying applicable clinical research regulatory, In depth therapeutic and protocol knowledge
What You'll Do.
Perform site selection visits
Perform site initiation visits
Perform site monitoring visits
Perform site close-out visits
Adapt subject recruitment plans
Drive subject recruitment plans
Track subject recruitment plans
Administer protocol training
Administer study training
Establish communication lines
Evaluate study site practices quality
Evaluate study site practices integrity
Manage study progress
Track regulatory submissions
Track regulatory approvals
Track data query generation
Track data query resolution
Create site management documentation
Create monitoring visit findings documentation
Create action plan documentation
How You'll Work.
Communication Scope
English; Spanish
Full Job Description
# **********Join us in our exciting journey!!********** We currently require a motivated, creative and enthusiastic clinical trials professional to join our rapidly growing Site Management division. As an experienced **Clinical Research Associate** , you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; we do not believe in a ‘career ceiling.’ IQVIA is expanding in Spain - we currently have multiple exciting vacancies for ********Clinical Research Associates 2 to work Full Services model**** ****to work with our key pharmaceutical clients****. If you have independent site monitoring experience as CRA and want to discover how a true partnership between the CRO and sponsor works, then this is the right opportunity for you! _Our clients are pharmaceutical companies who are dedicated and passionate about improving the lives of patients across several therapeutic areas._ **_The role: Responsibilities_** * Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans. * Administer protocol and related study training to assigned sites and establish regular lines of communication. * Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations – escalating quality issues as appropriate. * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. * Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans _**Our ideal candidate: Skills & other requirements**_ * In depth knowledge and skill i
Applying for this Clinical Research Associate 2 role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Iqvia?
Real rants from real employees. Read before you apply.