Senior Clinical Research Associate - Spain (Madrid)

Senior Clinical Research Associate - Spain (Madrid)

29 ago
|
Optimapharm
|
Madrid

29 ago

Optimapharm

Madrid

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 general 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 elevate potential risks and identify retraining opportunities
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.
Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.
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📌 Senior Clinical Research Associate - Spain (Madrid)
🏢 Optimapharm
📍 Madrid

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