Senior Clinical Research Associate - Spain

Tamarind Intelligence; Madrid; Híbrido; EUR 42.000 - 64.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Performance bonus

Referral bonus

Flexible work hours

Work from home allowance

Health Insurance

Descripción de la vacante

Optimapharm is seeking a CRA in Spain (Madrid/Barcelona based) to perform routine site visits, monitor trials, and ensure data integrity across studies.

Requirements include a medical/pharmacy degree and at least 4 years of independent monitoring experience, with fluency in English and the local language. The role offers growth opportunities, flexible hours, and a work-from-home allowance.

Formación

• University degree in medicine, pharmacy, dentistry, or equivalent.
• At least 4 years of independent clinical trial monitoring experience.
• Fluent in local language and English, both written and verbal.

Responsabilidades

• Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits across the region.
• Manage assigned sites by regular contact with site personnel to ensure site compliance and adequate enrolment.
• Independently perform CRF review and resolve data queries.

Conocimientos

Site monitoring

Good Clinical Practice

English proficiency

Interpersonal skills

Educación

Medical/Pharmacy degree

Herramientas

Data review systems

Documentation and CAPA

Descripción del empleo

Location: Spain (Madrid or Barcelona based)

Who we are?

Optimapharm is a mid-sized, global Contract Research Organisation turning science into hope through agile, patient-focused clinical development. At Optimapharm, you’ll have the opportunity to work on diverse and meaningful projects that help bring innovative therapies to patients worldwide. As part of our international team, you’ll collaborate with experts across multiple disciplines, gain exposure to a broad range of therapeutic areas, and contribute to research that makes a real difference.

With colleagues in 26 countries and operations in more than 40 countries, we combine global reach with the agility, collaboration, and supportive culture of a mid-sized organisation. Here, your expertise is valued, your growth is encouraged, and your work has a visible impact.

We’re searching for a CRA who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives . At Optimapharm, your dedication is rewarded with meaningful growth opportunities, exposure to diverse studies, and the support needed to reach your full potential.

What do we offer?

• Working in a successful company that’s growing and developing every day
• Being part of a clinical research team that transforms science into hope for patients
• International projects and professional growth
• Performance bonus
• Referral bonus
• Flexible work hours
• Work from home allowance
• Additional Health Insurance
• Shopping discounts
• Employee engagement programs
• Well-being initiatives
• Training and development program

Who are we looking for?

Qualifications And Experience

• University degree in medicine, pharmacy, dentistry, or equivalent
• At least 4 years of independent clinical trial monitoring experience (oncology, neurology, infectious diseases experience is a plus)
• Strong interest in clinical research and excellent understanding of the clinical trial process
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Fluent in local language and English, both written and verbal
• Computer proficiency is mandatory
• Ability to read, analyze, and interpret common scientific and technical journals
• Excellent verbal and written communication skills
• Excellent interpersonal and negotiation skills
• Ability to work with minimal supervision, pro-active
• Affinity to work effectively and efficiently in a matrix environment
• Excellent numerical skills and reasoning ability
• A current, valid driver's license

Your responsibilities

• Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits across the region
• Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements
• Independently perform CRF review; generate and resolve queries against established data review guidelines or data management systems as applicable
• Identify and escalation potential risks and identify retraining opportunities for site personnel
• Prepare corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow-up on each individual CAPA until timely resolution
• Prepare documents required for EC submissions and notifications, translate study-related documents (where applicable), and perform other tasks as instructed by the supervisor
• Independently negotiate study budgets with potential investigators and institutions and assist with the execution of site contracts as applicable
• Support administration of site payments in accordance with relevant project instructions

Compensation is competitive and final offers will reflect each candidate's experience, skills, and qualifications.