Senior Associate Audit - Uge Cat

Anonymous; Barcelona; On-site; EUR 50,000 - 70,000; Full time

Job summary

IQVIA Spain is seeking a Senior Clinical Research Associate 1 for sponsor-dedicated roles in Madrid and Barcelona. The position is full-time and requires on-site monitoring across sites, with exposure to multiple therapeutic areas and direct customer interaction.

You will conduct site visits, support recruitment planning, ensure regulatory compliance (GCP/ICH), manage progress, and collaborate with site teams and client representatives to drive study success while building expertise and

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 (GCP & ICH).
• Excellent MS Office skills.
• Fluent in Spanish and English.
• Strong organizational and time management abilities.
• Able to establish and maintain effective working relationships with coworkers, managers, and clients.
• Willingness and ability to travel.

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits
• Supporting development of a subject recruitment plan
• Evaluating site practices for compliance with GCP and ICH
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data queries
• Collaborating with study-site experts and client representatives

Skills

On-site monitoring

Regulatory knowledge

MS Office

Languages: Spanish & English

Time management

Relationship building

Travel flexibility

Driver's license

Education

University degree in scientific discipline or health care

Tools

MS Office

Job description

Senior Clinical Research Associate 1 - Sponsor dedicated

Madrid, Spain
Barcelona, Spain
Full time
R
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 package