Site Monitor I or II, FSP - Germany/Single Sponsor
Jetzt bewerben
Site Monitor I or II, FSP - Germany/Single Sponsor

Site Monitor I or II, FSP - Germany/Single Sponsor

Vollzeit 36000 - 60000 € / Jahr (geschätzt) Kein Home Office möglich
Jetzt bewerben
Parexel

Auf einen Blick

  • Aufgaben: Monitor clinical sites, ensuring data integrity and compliance with protocols.
  • Arbeitgeber: Join Parexel FSP, a leader in biopharmaceutical innovation dedicated to improving patient lives.
  • Mitarbeitervorteile: Enjoy remote work flexibility, exceptional financial rewards, and professional development opportunities.
  • Warum dieser Job: Be part of a mission-driven team that shapes groundbreaking solutions for global health.
  • GewĂĽnschte Qualifikationen: 1+ years as a clinical monitor; Bachelor’s degree or RN required.
  • Andere Informationen: Experience in Oncology or high-risk protocols is a plus. Apply today!

Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.

Parexel FSP is hiring for a home-based Clinical Site Monitor I or II.

Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients’ lives. Their daily innovation contributes to a healthier global community. This is where today’s visionaries, solution-seekers, and trailblazers converge to shape tomorrow’s groundbreaking solutions. Together, we have the power to revolutionize patients’ well-being. Every choice and step we make is guided by our unwavering focus on patients, fostering an environment where innovation thrives.

Experience Required:

The Site Monitor will be responsible for data integrity and data quality and will ensure compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for most activities to supplement on-site visit requirements. The Site Monitor will collaborate with the Site Manager to ensure that the site follows the protocol and is inspection-ready and will coordinate with institutions and investigators at the local level.

Qualifications:

  1. A minimum of 1 year’s experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite).
  2. Experience in managing complex protocols in Oncology or other therapeutic areas (TAs) where protocols are determined to be high risk.
  3. Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.
  4. Experience in utilizing systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence).

We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.

Apply today!#J-18808-Ljbffr

Site Monitor I or II, FSP - Germany/Single Sponsor Arbeitgeber: Parexel

At Parexel FSP, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration. Our commitment to employee growth is reflected in our comprehensive training programs and the opportunity to work with a leading biopharmaceutical company dedicated to improving patient lives. With a focus on work-life balance and competitive financial rewards, joining our team as a Site Monitor I or II means becoming part of a mission-driven organization where your contributions truly matter.
Parexel

Kontaktperson:

Parexel HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: Site Monitor I or II, FSP - Germany/Single Sponsor

✨Tip Number 1

Familiarize yourself with ICH GCP guidelines and local regulations. Understanding these standards will not only help you in your role but also demonstrate your commitment to compliance during the interview process.

✨Tip Number 2

Highlight your experience with virtual monitoring tools and systems like Siebel CTMS and eTMF. Being well-versed in these technologies is crucial for the Site Monitor position, and showcasing this knowledge can set you apart from other candidates.

✨Tip Number 3

Prepare to discuss specific examples of how you've managed complex protocols, especially in Oncology or high-risk therapeutic areas. This will illustrate your capability to handle the challenges that come with the role.

✨Tip Number 4

Emphasize your collaborative skills, particularly your ability to work with site managers and investigators. The role requires strong teamwork, so sharing experiences where you've successfully collaborated will be beneficial.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Site Monitor I or II, FSP - Germany/Single Sponsor

Clinical Monitoring
Data Integrity
Data Quality Assurance
ICH GCP Compliance
Study Monitoring Plan (SMP)
Virtual Monitoring Techniques
Oncology Protocol Management
Risk Assessment in Clinical Trials
Collaboration with Site Managers
Inspection Readiness
Communication Skills
Problem-Solving Skills
Experience with Siebel CTMS
Familiarity with eTMF and eISF Systems
Attention to Detail

Tipps für deine Bewerbung 🫡

Understand the Role: Make sure to thoroughly read the job description for the Site Monitor I or II position. Understand the key responsibilities, required qualifications, and the importance of data integrity and compliance with ICH GCP.

Highlight Relevant Experience: In your application, emphasize your experience as a clinical monitor, especially if you have worked with complex protocols in Oncology or other high-risk therapeutic areas. Be specific about your monitoring experience, whether virtual or onsite.

Showcase Technical Skills: Mention your familiarity with systems like Siebel CTMS, eTMF, and eISF. Providing examples of how you've utilized these systems in past roles can strengthen your application.

Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for improving patients' lives and your commitment to innovation in clinical monitoring. Tailor it to show how your values align with those of Parexel FSP.

Wie du dich auf ein Vorstellungsgespräch bei Parexel vorbereitest

✨Understand the Role and Responsibilities

Make sure you have a clear understanding of the Site Monitor position, including the importance of data integrity and compliance with ICH GCP. Familiarize yourself with the specific requirements of the role, such as monitoring protocols in Oncology or other therapeutic areas.

✨Showcase Your Experience

Be prepared to discuss your previous experience as a clinical monitor, especially any complex protocols you've managed. Highlight your familiarity with virtual monitoring and any relevant systems like Siebel CTMS or eTMF, as this will demonstrate your capability for the role.

✨Emphasize Collaboration Skills

Since the role involves working closely with Site Managers and local investigators, be ready to provide examples of how you've successfully collaborated in past roles. This could include discussing how you ensured sites were inspection-ready or how you coordinated with different stakeholders.

✨Prepare Questions for the Interviewers

Having thoughtful questions prepared shows your interest in the company and the role. Consider asking about the company's approach to innovation in patient care or how they support their employees' professional development, which aligns with their focus on fostering an environment where innovation thrives.

Site Monitor I or II, FSP - Germany/Single Sponsor
Parexel
Jetzt bewerben
Parexel
  • Site Monitor I or II, FSP - Germany/Single Sponsor

    Vollzeit
    36000 - 60000 € / Jahr (geschätzt)
    Jetzt bewerben

    Bewerbungsfrist: 2026-12-18

  • Parexel

    Parexel

    5000 - 10000
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