CTA Line manager/CTA Associate Line Manager (G140/150) (R1099512)

Job Description

IQVIATM is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

PURPOSE
Manage team/directs and overall activities for Site Management component of designated projects within the country, region or function, in accordance with the scope of work and contracted timelines in line with clinical monitoring portion of the study budget. Ensure that clinical staff (Clinical Trials Assistants -CTAs-) gains the necessary skills to perform their respective job responsibilities. Ensure the operational integration of department goals and objectives.

RESPONSIBILITIES
 Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters.
 Participate in the selection and on-boarding process for new clinical staff by conducting candidate review and participating in the interviewing process. Conduct on-boarding training for new staff in conjunction with Human Resources and Learning and Development training programs.
 Ensure that staff has the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and mentored training experiences, as applicable.
 Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies that are appropriate to their experience and training.
 Manage the quality of assigned staff's clinical work through regular review and evaluation of work product.
 Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.
 Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management.
 May participate in clinical operations quality or process initiatives.

All responsibilities are essential to job functions unless noted as non-essential (N).

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

 eTMF expertise, highly valued.

 Advanced knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
 Strong leadership skills.
 Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
 Strong written and verbal communication skills including good command of English.
 Excellent organizational and problem solving skills.
 Effective time management skills and ability to manage competing priorities.

 Ability to establish and maintain effective working relationships with coworkers, managers and clients.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
 Bachelor's degree in a health care or other scientific discipline or educational equivalent; 7 yrs of clinical trials experience including 2 years experience in a leadership capacity; or equivalent combination of education, training and experience”

100% office based role > IQVIA offices: Retiro, Buenos Aires.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.