דלג לתוכן הראשי

Senior Clinical Research Associate - Isreal - Oncology - FSP

ParexelישראלמרחוקFull-timeדרגה: בכיר/ה

פורסם לפני 17 ימים · 31 מועמדים

שכר לא צוין במשרה זו

שמירה, הגשה או בדיקת התאמה — כמה שניות להקמת חשבון חינם.

תובנת Willbi

התפקיד במילים פשוטות

This role involves managing and supervising all site activities for assigned oncology clinical studies. You will work from a home office, supporting studies within your country or region, and will be dedicated to a single client.

חובה
  • Extensive experience in site management, with knowledge of clinical trial methodology and terminology.
  • Minimum 5 years’ experience in independent supervision of all types of visits.
  • Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities.
  • Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.
יתרון
  • opportunity to mentor junior CRAs

חולץ מתיאור המשרה · מתעדכן אוטומטית

למי זה מתאים

This role suits individuals with extensive experience in site management and oncology trials, specifically at least five years in each area, including independent supervision of all visit types. It is ideal for those who can effectively manage their time, prioritize tasks, and possess a strong understanding of clinical research methodology and regulations.

תיאור המשרה המלא

המשרה המקורית · נשמר לעיון

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at SCRA, home-based, Isreal.

We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.

As the company that conducts vital clinical studies for sponsors, including the world's leading biotech’s and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.

Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

The most significant aspect of this position is that

You will be dedicated to a single client

You will be responsible for all site management and supervisory activities in the assigned oncology studies.

You will work with industry leaders and subject matter experts.

You will have the opportunity to mentor junior CRAs.

You will work with world-class technology.

You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

From you we expect

Extensive experience in site management, with knowledge of clinical trial methodology and terminology.

Experience in oncology trials, at least 5 years.

Minimum 5 years’ experience in independent supervision of all types of visits.

Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities.

Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.

We will offer you

Premium salary.

Attractive benefits.

Car or company car

Medical care plan: Health, Dental & Vision.

Life Assurance.

Excellent work environment.

Culture of teamwork and collaboration.

People who motivate and face challenges together.

Innovative technology.

Excellent training.

Our people and their passion are very important to us as they are the key to our success. That's why we provide you with an open and friendly working environment where we empower people and provide them with opportunities to develop their careers in the long term. In addition, you will have the opportunity to develop within your role and take on more responsibility or develop your skill set within other related Parexel FSP departments.

For an immediate interview, please contact marta.kuniewicz@parexel.com

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אודות Parexel
פרופיל החברה · בקרוב

ביקורות עובדים · בקרובעוד משרות ב-Parexel

שאלות על המשרה

  • המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
Parexel
פורסם לפני 17 ימים · 31 מועמדים