The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, with offices located in France, UK, US, Belgium, Denmark, Sweden, Switzerland, Romania, and India.
The CRO occupies a unique position in the clinical research industry, supporting biotech in clinical trials across all phases (Ph. I - IV) and non-interventional studies, as an expert in the operational delivery of clinical trials. Our vision is to conduct clinical trials better than anyone else, to help patients and ultimately save lives. We have earned a strong reputation for successfully delivering complex, demanding and innovative clinical trials, with specialist therapeutic expertise in oncology, cell & gene therapy, radiopharmaceuticals and rare diseases.
We are currently looking for an enthusiastic and talented
Legal Site Agreement Specialist . This role can be permanent/fixed-term/freelance and home-based in the UK or EU where we have the ability to hire. Key responsibilities
Legal Site Agreement Specialist will support the General Counsel on various contracts review process focusing on clinical site agreements, feasibility NDAs, CDAs and other commercial agreements, and will be responsible for reviewing, editing, and drafting various commercial agreements. You must be able to take in large documents and understand legal contracts in a business to business setting within the clinical trials industry. Qualifications and attributes:
Minimum of 2 years hands-on experience reviewing clinical site contracts in a pharma or CRO environment General commercial contracts experience within a clinical trials environment Strong appreciation of contract law with a good legal understanding from previous in-house experience in a contracts role Previous exposure of dealing with sites and investigators located in EU and the USA highly desirable Excellent communication skills, both written and verbal in English with second European language desirable Strong attention to detail and proven drafting skills Available to start immediately or at short notice What we offer:
Opportunity to be part of an innovative organization and work with exciting technologies Mentorship and training to further develop your skills in the clinical trials industry Competitive employment package
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Legal Site Agreement Specialist . This role can be permanent/fixed-term/freelance and home-based in the UK or EU where we have the ability to hire. Key responsibilities
Legal Site Agreement Specialist will support the General Counsel on various contracts review process focusing on clinical site agreements, feasibility NDAs, CDAs and other commercial agreements, and will be responsible for reviewing, editing, and drafting various commercial agreements. You must be able to take in large documents and understand legal contracts in a business to business setting within the clinical trials industry. Qualifications and attributes:
Minimum of 2 years hands-on experience reviewing clinical site contracts in a pharma or CRO environment General commercial contracts experience within a clinical trials environment Strong appreciation of contract law with a good legal understanding from previous in-house experience in a contracts role Previous exposure of dealing with sites and investigators located in EU and the USA highly desirable Excellent communication skills, both written and verbal in English with second European language desirable Strong attention to detail and proven drafting skills Available to start immediately or at short notice What we offer:
Opportunity to be part of an innovative organization and work with exciting technologies Mentorship and training to further develop your skills in the clinical trials industry Competitive employment package
#J-18808-Ljbffr
