Senior Clinical Research Associate 1 - Sponsor dedicated

IQVIA; Madrid; Hybrid; EUR 40,000 - 50,000; Full time

Benefits offered by this job

Career growth resources

Flexible work schedules

Attractive benefits package

Mobile phone

Job summary

A leading clinical research organization is seeking a Senior Clinical Research Associate 1 in Madrid. You'll perform site-related tasks including selection and monitoring, while ensuring compliance with regulatory standards. A university degree and at least 2 years of experience in on-site monitoring are required. This position offers flexible work schedules and support for career growth in a global organization committed to improving health outcomes.

Qualifications

• University degree in scientific discipline or health care.
• At least 2 years of on-site monitoring experience.
• Good knowledge of clinical research regulatory requirements.
• Excellent command of Spanish and English language.

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.
• Managing progress by tracking regulatory submissions and data query resolution.
• Collaborating with experts at study sites and with client representatives.

Skills

On-site monitoring experience

Knowledge of regulatory requirements

Computer skills including MS Office

Excellent command of Spanish

Excellent command of English

Organizational skills

Time management skills

Problem-solving skills

Education

University degree in scientific discipline or health care

Job description

Senior Clinical Research Associate 1 - Sponsor dedicated page is loaded## Senior Clinical Research Associate 1 - Sponsor dedicatedlocations: Madrid, Spain: Barcelona, Spaintime type: Full timeposted on: Posted Todayjob requisition id: R1530988**Senior Clinical Research Associate 1**IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.When you join **IQVIA Spain** as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.With access to world-class training and mentoring, you’ll 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.**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 (GCP) and International Conference on Harmonization (ICH) guidelines* Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution* Collaborating with experts at study sites and with client representatives**Qualifications:*** University degree in scientific discipline or health care* At least 2 years of on-site monitoring experience* Good knowledge of clinical research regulatory requirements* 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* Better Work-Life balance, optimal DOS* 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 .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.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.