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HERAX is looking for outgoing and talented Life Science, CBS or IT graduates with preferably 1-2 years of experience due to continual growth in our Life Sciences business areas. Our new consultants should be team players with strong interpersonal and analytical skills, and a wish to undergo a steep learning curve.
As a Pharma Business consultant, you will be part of a team working together in planning and executing projects. You will be involved in every step of the projects from the idea phase (business case development) to identifying the value adding areas, analyzing current and future processes and technology as well as designing and delivering solutions.
We offer an exciting job with excellent development opportunities in a young, dynamic, and informal environment, where our colleagues are passionate about their work and great at celebrating our successes.
Genmab A/S, Copenhagen
We are looking for an experienced and dedicated Lead Clinical Research Associate (Lead CRA) to be part of Global Clinical Operations at our Headquarters in Copenhagen.
As Lead CRA you will be responsible for the planning, conduct and coordination of trial oversight activities with internal and external stakeholders to ensure quality and integrity of the data within and across Genmab clinical trials. In addition you will support the Clinical Trial Manager (CTM) with identification of investigators, build relationship with investigators/trial sites and conduct sponsor site visits to support recruitment and ensure compliance.
You will support the CTM in securing timely delivery and review of trial related documents, plans including but not limited to master PI/ICF, training records and monitoring visit reports, attend PTVs and SIVs and perform ongoing co-monitoring of the trials.
LEO Pharma, Ballerup
Would you like to play a key role in the development of our growing portfolio with a friendly, ambitious and professional team of Clinical Trial Supply Professionals?
As a Clinical Trial Supply Professional you will join a very dedicated team, who is responsible for coordinating IMP outsourced related activities in connection with the conduct of Clinical Trials Phase I-IV. You will be working according to given LEO Pharma procedures and relevant GMP, GCP and regulatory requirements. You will also:
- Have a strong understanding for IRT/IWR systems
- Provide input to the Clinical Trial Protocol
- Create SOP's and keep them updated.
Nordic Bioscience A/S, Herlev
Nordic Bioscience Clinical Development (NBCD) is an international drug development organization. We believe that personalized medicine and innovation in study design and conduct is the key to developing new drugs smarter, better and faster.
As a result of our continued growth, we are now looking for a person to be a part of our CRA team in Herlev.
Your job as Clinical Research Associate is highly varied and will amongst other responsibilities include the following:
- You will act as liaison between the sponsor and the investigator and play a very important role in motivation of the investigators at the clinics and in ensuring patient safety and data integrity.
- You will perform on-site monitoring of the trials performed by NBCD according to ICH-GCP.
- Assist Clinical Trial Managers in ad hoc study management related tasks, which will be tailored to your wishes and your skills (or desired skills).