Senior Clinical Research Associate 1 - Sponsor dedicated

3M HEALTHCARE; Barcelona; Presencial; EUR 42.000 - 64.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Mobile phone included

Excellent benefits package

Descripción de la vacante

IQVIA in Barcelona is seeking a Senior Clinical Research Associate to join our sponsor-dedicated CRA team. You will support multicenter trials, perform site visits, and help ensure GCP/ICH compliance throughout study conduct.

Responsibilities include site initiation, monitoring, close-out visits, and managing recruitment plans. Strong English/Spanish, MS Office, and travel flexibility are essential to succeed in this role.

Formación

• 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.

Responsabilidades

• 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 ICH guidelines.
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
• Collaborating with experts at study sites and with client representatives.

Conocimientos

Spanish language

English language

Driver’s license Class B

Travel flexibility

MS Office proficiency

Educación

University degree in scientific discipline or health care

Herramientas

MS Office

Descripción del empleo

Senior Clinical Research Associate

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 package

IQVIA 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.