Clinical Research Specialist II

vor 3 Wochen

Frankfurt am Main, Deutschland Pharmiweb Vollzeit

Position Overview:
As a Clinical Research Specialist II or Senior Clinical Research Specialist, you will be engaged in a home-based role across Germany. At Pharmiweb, our workforce is our greatest asset, and it is our diverse teams that empower us to be a superior partner to our clients, fulfilling our mission to enhance and improve patient outcomes.

Our Core Values:
Our culture is built on four fundamental values that unite us as individuals and distinguish us as an organization:
• Accountability & Delivery
• Collaboration
• Partnership
• Integrity

We aspire to be the Clinical Research Organization that consistently delivers excellence to our clients and to patients at every interaction. This vision drives us, and we seek talented individuals who share this commitment. If you are as passionate as we are, we invite you to join our team.

Work Environment:
You will thrive in a dynamic and supportive atmosphere, collaborating with some of the brightest and most amiable professionals in the industry, while contributing to the evolution of the sector.

Key Responsibilities:
As a Clinical Research Specialist at Pharmiweb, you will:

  • Conduct independent and proactive tasks to establish and oversee studies, complete reports, and maintain essential documentation.
  • Prepare and submit protocol and consent documents for ethics/IRB approval, along with regulatory submissions.
  • Manage sponsor-generated inquiries effectively.
  • Ensure cost efficiency throughout the study lifecycle.
  • Prepare and review study documentation and feasibility assessments for new proposals.
  • Possibly assist in the training and mentoring of junior Clinical Research Specialists.

Qualifications:
To be successful in this role, you will need:

  • A minimum of 18 months of monitoring experience in phase I-III clinical trials.
  • A college degree in medicine, science, or a related field.
  • Prior experience in monitoring medium-sized studies, including study initiation and closure.
  • Familiarity with ICH-GCP guidelines and the ability to review and assess medical data.
  • Exceptional written and verbal communication skills.
  • The capability to meet tight deadlines.
  • Willingness to travel at least 60% of the time (both internationally and domestically) and possess a valid driving license.

Benefits of Joining Pharmiweb:
Our success is contingent upon the caliber of our personnel. Therefore, we prioritize cultivating a culture that rewards high performance and nurtures talent. We offer competitive salary packages, regularly benchmarking them against industry standards. Our annual bonuses reflect the achievement of performance objectives—both organizational and individual.

Additionally, we provide a comprehensive range of health-related benefits for employees and their families, along with competitive retirement plans and related benefits such as life assurance, enabling you to save and plan confidently for the future.

Beyond competitive salaries and extensive benefits, you will find an environment that encourages you to fulfill your sense of purpose and drive meaningful change.

Pharmiweb is an equal opportunity and inclusive employer, dedicated to providing a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

If you require reasonable accommodation due to a medical condition or disability during the application process or to perform essential job functions, please inform us through the appropriate channels.

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