Site Engagement Specialist

Tamarind Intelligence

Barcelona

Híbrido

EUR 42.000 - 65.000

Jornada completa

Hace 6 días
Sé de los primeros/as/es en solicitar esta vacante
Generador de candidaturas

Una candidatura hecha para este puesto de trabajo: un currículum y una carta de presentación adaptados que responden directamente a la oferta.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Hybrid working model
Private health Insurance (AXA)
Birthday day off
Wellhub (GymPass)
Flexible compensation plan (Cobee)
MacBook computer

Descripción de la vacante

MEDSIR, a Barcelona-based company, seeks a Site Engagement Specialist to design and optimize patient recruitment strategies for oncology trials. You will collaborate with site staff, investigators, and internal teams to ensure enrollment targets are met on time while adhering to GCP and regulatory requirements.

The role emphasizes building strong PI and site engagement, developing customized recruitment plans, and analyzing recruitment data to drive improvements.

Formación

  • Bachelor's degree in Life Sciences, Clinical Research, Pharmacy, or related field.
  • Strong understanding of GCP, ICH guidelines, and regulatory requirements.
  • Experience in stakeholder engagement, site collaboration, and recruitment optimization.
  • Demonstrated ability to develop and implement effective patient recruitment plans.
  • Strong analytical and problem-solving skills to assess recruitment trends and drive improvements.
  • Excellent communication and interpersonal skills.
  • Experience in conducting surveys and analyzing recruitment data.
  • Strong organizational and time management skills to ensure oversight of trial recruitment activities.
  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
  • Fluency in English and Spanish.
  • Availability to travel, as required by study needs.

Responsabilidades

  • Develop and implement patient recruitment plans based on trial objectives and site capabilities.
  • Engage with Principal Investigators, Sub-Investigators, and site coordinators to share best practices.
  • Identify and engage community organizations and healthcare networks to support recruitment.
  • Monitor recruitment activities across sites and take corrective actions to maintain momentum.
  • Collect and analyze recruitment metrics to identify trends and improvements.
  • Collaborate with study teams to share best practices and implement process improvements to boost recruitment.

Conocimientos

English fluency
Spanish fluency
Stakeholder engagement
Recruitment optimization
Analytical skills
MS Office

Educación

Bachelor's degree in Life Sciences

Descripción del empleo

WHY CHOOSE MEDSIR

We are a Barcelona-based fastest-growing company founded by scientific experts . We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results . Together, we create the best strategies that are both clinically relevant and scientifically meaningful . We strive to improve our knowledge of this complex disease and the vast array of available treatments in a fast-innovative way .

At MEDSIR, you will have the job of your life while working together towards our shared mission bringing novel treatments to cancer patients worldwide. We welcome top performers that will bring new ideas, diverse perspectives, and provide you the opportunities and freedom to grow and make a real impact in patients' lives and science... all while having great fun .

ABOUT THE OPPORTUNITY

The Site Engagement Specialist plays a pivotal role in designing, implementing, and refining patient recruitment strategies for clinical trials. By collaborating closely with site staff, investigators, and internal teams, the SES ensures that enrollment targets are met within established timelines. This position demands a solid understanding of Good Clinical Practices (GCP) and regulatory requirements, as well as a focus on patient-centric approaches to enhance recruitment quality and efficiency .

HOW YOU WILL CONTRIBUTE:
  • Develop and Implement Patient Recruitment Plans : Formulate customized recruitment plans based on trial objectives, patient profiles, and site capabilities. Regularly refine these plans using metrics and stakeholder feedback to ensure enrolment goals remain achievable and aligned with overall trial strategies .

  • Site and Investigator Engagement : Establish and maintain ongoing communication channels with Principal Investigators (PIs), Sub-Investigators (Sub-Is), and site coordinators. Provide tools, resources, and best practices tailored to each site's unique environment, focusing on strengthening site-level ownership of recruitment goals .

  • Stakeholder Identification and Collaboration : Identify and engage community organizations, advocacy groups, and healthcare networks that can support trial awareness and patient outreach. Work closely with internal teams---such as medical affairs and marketing---to leverage educational materials, events, and digital platforms that highlight trial opportunities .

  • Patient Recruitment Oversight: Monitor recruitment activities across sites, analyzing patient enrollment trends in real time. Ensure that any corrective actions are promptly executed to maintain momentum .

  • Performance Analysis and Reporting : Collect and analyze recruitment metrics--- such as screen-failure rates, referral sources, and enrollment ratios---to identify trends and potential areas of improvement. Provide regular updates to management, highlighting successes, challenges, and recommended solutions to optimize recruitment outcomes .

  • Site-Level Recruitment Optimization : Collaborate with investigators and study teams to share best practices, enhance site engagement, and implement process improvements. Offer guidance on pre-screening methods, patient education materials, and innovative communication strategies to boost patient interest and retention .

  • Leadership in Stakeholder Engagement : Act as a unifying force among site personnel and internal teams, fostering collaboration and alignment on recruitment objectives. Organize and moderate roundtable discussions or workshops, where stakeholders can exchange insights on patient outreach methods and address hurdles collectively .

  • Addressing Recruitment Barriers : Diagnose and resolve site-specific challenges--- such as protocol complexity, logistical constraints, or limited patient pools---by proposing tailored action plans .

  • Milestone Tracking and Proactive Issue Resolution : Set clear enrollment milestones and report on progress to key stakeholders. Identify potential risks to recruitment timelines, escalating them as necessary and recommending solutions that maintain study progress while protecting data integrity and patient safety .

  • Training and Knowledge Sharing: Develop and deliver engaging training sessions to equip site staff with effective patient engagement and retention strategies. Continuously review training content to ensure compliance with evolving regulations, best practices, and feedback from recently concluded or ongoing trials.

WHAT DO WE VALUE FOR THIS OPPORTUNITY?
  • Bachelor's degree in Life Sciences, Clinical Research, Pharmacy, or a related field .

  • Strong understanding of Good Clinical Practices (GCP), ICH guidelines, and regulatory requirements .

  • Experience in stakeholder engagement, site collaboration, and recruitment optimization .

  • Demonstrated ability to develop and implement effective patient recruitment plans .

  • Strong analytical and problem-solving skills to assess recruitment trends and drive improvements .

  • Excellent communication and interpersonal skills .

  • Experience in conducting surveys and analyzing recruitment data .

  • Strong organizational and time management skills to ensure effective oversight of trial recruitment activities .

  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, Outlook) .

  • Fluency in English and Spanish .

  • Availability to travel, as required by study needs .

  • Excellent organizational skills with demonstrated ability to execute support on projects on time and on budget.

THE THINGS YOU REALLY WANNA KNOW :

At MEDSIR, we believe that employees today want to evolve in collaborative, high-growth environments where they can demonstrate their abilities and thrive both professionally and personally. We are convinced that employees need to find alignment between their inner values and their company's culture and mission to unlock their full potential. We work to create a culture of empowerment, continuous learning and growth where everyone can bring expertise, own projects and easily measure their impact .

BENEFITS

Work with world-renowned clinicians and KOL's on high-level publications and papers .

Fast growth, we are an early-stage company with a multidisciplinary team and many growth opportunities .

Work-life balance - hybrid working model and flexible hours focusing on performance rather than office hours .

Unlimited access to GoodHabitz courses and regular workshops (external & internal) to continue your development .

Opportunities to participate in scientific conferences & events at national and international level .

Private health Insurance (AXA) .

Work-from-abroad policy depending on position and local legislation .

A young & international team with a company culture focused on development .

Positive, dynamic, and passionate work environment .

Elevate your wellness with Wellhub (formerly GymPass)! One subscription for the best in fitness, mindfulness, therapy, nutrition, and sleep support---all in one place .

"Flexible compensation plan" to help you save taxes and increase your net salary (Cobee) .

A free day on your birthday so you can truly celebrate!

Unforgettable MEDSIR events and regular get togethers .

Equal employment opportunity, at MEDSIR we proudly pursue a diverse workforce and celebrate our differences .

A fantastic workplace located in 22@, Barcelona's new hub of innovation .

We work with MacBook computer (Apple) .

If you believe you match our values, you are unique and feel ready to make a change, we look forward to meeting you!

We are committed to fostering a diverse and inclusive workplace, where all individuals are treated with respect and equality, regardless of race, gender, age, religion, disability, or any other characteristic. We believe in providing equal opportunities for all and do not tolerate discrimination in any form.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra y suelta tu archivo aquí
Similar jobs

Puestos de trabajo similares que vale la pena comparar

Site Engagement Specialist
Site Engagement Specialist

MEDSIR • Barcelona

Híbrido
EUR 42.000 - 64.000
Hybrid working model
Private health Insurance
Wellbeing programs
Trainee Clinical Trial Protocol Writer
Trainee Clinical Trial Protocol Writer

MEDSIR • Barcelona

Híbrido
EUR 18.000 - 24.000
Hybrid working model
Study compensation for transport and食
MacBook provided (Apple)
+4
Biostatistician trainee
Biostatistician trainee

MEDSIR • Barcelona

Presencial
EUR 13.000 - 18.000
Hybrid working model
Study compensation support
Work with KOLs on publications
+4
Clinical Trial Site Relationship Coordinator
Clinical Trial Site Relationship Coordinator

Medpace • Madrid

Presencial
EUR 42.000 - 62.000
Competitive compensation
Comprehensive health, retirement, and
WFH flexibility after training
Clinical Trial Site Relationship Coordinator
Clinical Trial Site Relationship Coordinator

Medpace, Inc. • Madrid

Presencial
EUR 42.000 - 64.000
Clinical Trial Site Engagement & Recruitment Lead
Clinical Trial Site Engagement & Recruitment Lead

MEDSIR • Barcelona

Híbrido
EUR 42.000 - 64.000
Hybrid working model
Private health Insurance
Wellbeing programs
Solution Lead - Study Design Platform
Solution Lead - Study Design Platform

Merck Healthcare • Mollet del Vallès

Presencial
EUR 90.000 - 150.000
Senior Clinical Research Associate - Spain
Senior Clinical Research Associate - Spain

Optimapharm • Madrid

Presencial
EUR 40.000 - 62.000
Performance bonus
Referral bonus
Flexible work hours
+6
Senior Clinical Research Associate - Spain
Senior Clinical Research Associate - Spain

Tamarind Intelligence • Madrid

Híbrido
EUR 42.000 - 64.000
Performance bonus
Referral bonus
Flexible work hours
+2
Solution Lead - Study Design Platform
Solution Lead - Study Design Platform

Biopharma Careers • Mollet del Vallès

Presencial
EUR 85.000 - 130.000