Clinical Research Associate 2 - CFSP

IQVIA LLC; España; On-site; PHP 2,109,704 - 3,013,864; Full time

Benefits offered by this job

Mobile phone

Attractive benefits package

Career growth resources

Support for flexible work schedules

Job summary

IQVIA LLC is seeking a motivated Junior Clinical Research Associate in the Philippines for supporting clinical trials. The ideal candidate will engage in site monitoring, initiate evaluations, and collaborate effectively with various stakeholders.

Applicants should possess a university degree in a scientific discipline or healthcare, have experience in the Pharma industry, and excel in both English and Spanish. The role offers flexibility to travel, an excellent working environment, and a robust benefits package.

Qualifications

• Experience in Pharma Industry, and/or Clinical Trials environment.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Flexibility to travel.

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements.

Skills

Excellent command of Spanish and English language

Strong organizational skills

Problem-solving skills

Time management skills

Very good computer skills including MS Office

Education

University degree in scientific discipline or health care

Job description

## Clinical Research Associate 2 - CFSPApplylocations: Madrid, Spain: Barcelona, Spaintime type: Full timeposted on: Posted Todayjob requisition id: R1530991**Clinical Research Associate****IQVIA Spain** is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.**Your responsibilities will include:*** Performing site selection, initiation, monitoring and close-out visits* Supporting the development of a subject recruitment plan* Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines* Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions* Collaborating with experts at study sites and with client representatives**Qualifications:*** University degree in scientific discipline or health care* Experience in Pharma Industry, and/or Clinical Trials environment* Very good computer skills including MS Office* Excellent command of Spanish and English language* Organizational, time management and problem-solving skills* Ability to establish and maintain effective working relationships with coworkers, managers, and clients* Flexibility to travel* Driver’s license class B**What you can expect:*** Resources that promote your career growth* Leaders that support flexible work schedules* Programs to help you build your therapeutic knowledge* Excellent working environment in a stabile, international, reputable company* Mobile phone and attractive benefits packageIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.