Evotec

Clinical Research Associate I

Evotec$90K — $110K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3+ years as Clinical Trial Assistant or CRA
  • Understanding of medical and pharmacological terminology
  • Knowledge of Good Clinical Practice (GCP) guidelines
  • Strong organizational and planning skills
  • Good communication and interpersonal skills
  • Experience with CROs
  • Experience maintaining eTMF preferred

Responsibilities

  • Assist with project management within the Clinical Development group
  • Collaborate with CROs during clinical trials
  • Schedule and manage meeting logistics
  • Prepare and archive clinical documentation
  • Monitor and QC the electronic Trial Master File (eTMF)
  • Serve as the main contact for project communications
  • Coordinate logistics for clinical trial operations

Benefits

  • Growth Opportunities: Focus on continuous learning and development
  • Flexible Work Environment: Options for hybrid work schedules
  • Inclusive Culture: Emphasis on diversity and curiosity
  • Innovative Projects: Work on groundbreaking initiatives
  • A Place for Big Ideas: Encouragement for creative thinking
Full Job Description
Job Title: Clinical Research Associate I

Location: Remote

Reports to: Head of Clinical Operations

The Role:

We're looking for a passionate and curious, CRA 1 to join our team. If you're excited by new challenges, to work as the lone CRA in a small clinical development group, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

As the CRA 1 at Just-Evotec, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team.

What You'll Do:
  • Assist with project management tasks within Clinical Development group
  • Collaborate with CRO(s) in the execution of clinical trials
  • Schedule meetings, set agendas, track action items and capture meeting minutes
  • Prepare, handle, distribute, file, and archive clinical documentation and reports
  • Monitor and QC the eTMF
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
  • Coordinate and manage logistical aspects of clinical trials, such as shipment of lab samples
  • Help monitor the progress of clinical trials, track timelines and ensure adherence to protocol and other study documentation
  • Assist in the preparation of regulatory submissions
  • May review and approve invoices, purchase orders and site payments
  • Identify and address potential risks to the project timeline, quality, or budget and escalate when necessary
  • Help manage relationships with external vendors, including CROs, laboratories, and other service providers
  • Help ensure all study materials are properly archived following the completion of a trial


Who You Are:
  • At least 3 years work experience as a Clinical Trial Assistant or CRA
  • Understanding of medical and pharmacological terminology
  • Knowledge of Good Clinical Practice (GCP) guidelines
  • Strong organizational and planning skills. Project management experience a plus
  • Good communication and interpersonal skills
  • Experience working with CROs
  • Experience maintaining eTMF preferred
  • Proficient with MS Project and/or Smartsheet preferred
  • Experience managing clinical lab samples a plus
  • Data review experience plus
  • BSc degree in life sciences or related field preferred


Why Join Us:
  • Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow.
  • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life, with hybrid work schedules in many of our various locations.
  • Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged.
  • Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
  • A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them.


Are You Still Curious?

If you've read this far, then chances are you've got a curious mind, just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you and how it will shape the future of Just-Evotec.

Let your curiosity guide your career. #BeCurious and explore the endless possibilities at Just-Evotec!

The base salary range for this position at commencement of employment is expected to be $90,000 - $110,000; Base salary offered may vary depending on individual's skills, experience and competitive market value.

About Evotec

Evotec is a drug discovery and development company that provides services to pharmaceutical and biotechnology companies. The company's services include drug discovery, preclinical development, and clinical development. Evotec was founded in 1993 and is headquartered in Hamburg, Germany.
Learn more about Evotec
Size
3,000 employees
Industry
Founded
1993

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