.Location: Madrid or BarcelonaWho are we?Optimapharm is a leading, mid-sized, full-service CRO working across Europe and North America to deliver new therapies to improve and save patients' lives.Optimapharm's key priorities are our people and consistently exceeding our client's expectations.
With 26 strategically located offices, Optimapharm operates in 40+ countries, giving unrivaled access to Patients and Investigators in all countries in Europe and North America.
In-depth expertise and long-standing experience, combined with a flexible and collaborative approach, allow optimization of design and planning; through its strong track record of delivery excellence and committed and stable project teams, Optimapharm has secured a high level of repeat business over the years.We are looking for an experienced Clinical Research Associate to join our Clinical Operations team in Spain (in Madrid or Barcelona) and support us in making a tangible difference to project sponsors and benefiting patients and their families all around the world.What do we offer?Working in a successful company that's growing and developing every dayWorking with a highly experienced team of clinical research professionalsInternational projects and professional growthPerformance bonusReferral bonusTraining opportunitiesFlexible work hoursMadrid location: home based + allowanceBarcelona location: work from home + allowanceAdditional Health InsuranceShopping discountsWho are we looking for?University degree, preferably in medical or life sciences.Individuals with university degree in biotechnical, technical, bio medicinal, social, or humanistic sciences must have nursing education or other relevant healthcare college degree.At least 4 years of individual clinical trial monitoring experience; Oncology and Phase I, or other complex study monitoring is an advantage.High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements, and a strong interest in clinical research.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.Very good interpersonal and negotiation skills.Ability to work with minimal supervision, proactive.Affinity to work effectively and efficiently in a matrix environment.Excellent numerical skills and reasoning ability.A current, valid driver's license would be advantageous.Your responsibilities:Perform routine site visits with minimal guidance, including pre-study, initiation, interim monitoring, and closeout visits.Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment, and understanding of study requirements.Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable