Current jobs related to Clinical Research Associate - Darwin, Northern Territory - Pharmiweb

We are seeking a highly skilled Clinical Research Associate to join our team in Germany. As a Senior CRA, you will be responsible for setting up and monitoring studies, completing reports, and maintaining documentation.

The ideal candidate will have at least 4 years of monitoring experience in phase I-III trials as a CRA and possess a degree in medicine, science, or equivalent. You should also have previous monitoring experience in medium-sized studies, including study start-up and close-out.

You will be working with one of the world's premier Biopharmaceutical companies, partnering on a vast portfolio of medicines and vaccines. Your responsibilities will include:

• Independent, proactive work to set up and monitor studies, complete reports, and maintain documentation
• Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
• Balancing sponsor generated queries
• Taking responsibility for study cost efficiency
• Preparation and review of study documentation and feasibility studies for new proposals
• Potential to assist in training and mentoring fellow CRAs

To succeed in this role, you will need:

• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Excellent written and verbal communication in both English and German
• Ability to work to tight deadlines
• Availability to travel at least 60% of the time (international and domestic)

In return, we offer a competitive salary of €60,000 - €80,000 per year, depending on experience, plus a range of benefits, including various annual leave entitlements, health insurance, retirement planning, and flexible country-specific optional benefits. Our company culture values diversity, inclusion, and belonging, and we are committed to providing an inclusive and accessible environment for all candidates.