Junior Project Manager in Clinical Research

vor 4 Wochen


Munich, Bayern, Deutschland Scienta Vollzeit

Junior Project Manager in Clinical Research (Oncology)

Location: Germany (Candidates can be located anywhere in Germany. Please note that relocation or sponsorship cannot be provided for this role).

About Scienta

Scienta is a pioneering organization in the field of oncology research, committed to the advancement of groundbreaking therapies that aim to transform cancer treatment. As we expand our immuno-oncology clinical initiatives, we are looking for a skilled Clinical Research Associate (CRA) in Germany who is ready to transition into a Junior Project Manager position.

Position Overview

If you are a Senior or Lead CRA with a strong interest in oncology and are eager to advance into a Clinical Project Management role, this opportunity is for you. In this position, you will play a crucial role in a growing biotech firm, overseeing and managing oncology clinical trials, initially within Germany and subsequently on a global scale. You will collaborate closely with cross-functional teams to facilitate the delivery of innovative cancer therapies to patients in need.

Key Responsibilities

  • Assist in the planning, execution, and oversight of oncology clinical trials from initiation to completion across Phases I-III.
  • Ensure that trials are conducted timely, within budget, and uphold the highest standards of quality and regulatory compliance.
  • Engage with internal and external stakeholders, including clinical operations, regulatory affairs, and study sites.
  • Monitor trial progress, identify challenges, and implement solutions to maintain project timelines.
  • Support the preparation and review of clinical protocols, informed consent documents, and other trial-related materials.
  • Serve as a primary contact for study sites and vendors, ensuring effective communication and problem resolution.
  • Contribute to regulatory submissions and liaise with ethics committees, ensuring all activities comply with GCP and other regulatory standards.

Qualifications

  • Bachelor's degree in Life Sciences or a related field.
  • Significant experience as a Senior or Lead CRA, particularly in oncology trials.
  • Comprehensive understanding of the oncology therapeutic area, clinical trial processes, and regulatory frameworks.
  • Exceptional organizational skills with the ability to manage multiple priorities in a dynamic environment.
  • Strong communication and interpersonal abilities.
  • Proactive mindset with a desire to learn and develop within a fast-paced biotech setting.
  • Fluency in both German and English.

Application Process

For a confidential discussion regarding this role, please reach out to us.


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