ORCHARD THERAPEUTICS PLC is looking for employees for positions:
business development manager
Working hours
full-time
Language
english
Responsibility
business Development
location: Boston, MA or London, UK
builds and delivers compelling, audience-specific scientific & business presentations for prospective partners
reporting to: VP, Head of Business Development
co-ordinates the due diligence process for in- and out-licensing activities with all relevant functions
competitive Intelligence Monitors existing and upcoming programs and technology in Orchard’s fields of interest and reports findings Working with the Program teams and Commercial development teams, contributes to providing up to date, comprehensive and informed overviews of Orchard program’s competitive positioning Derives insights and develops presentations and recommendations for the Executive Leadership Team
supports the structuring, negotiating and execution of term sheets and agreements
competitive Intelligence
Requirements
skills & Abilities
independent worker with strong organizational skills who can take strategy goals and work to execute them with minimum oversight
excellent communication and interpersonal skills to effectively convey key recommendations to senior management and potential partners of various cultural backgrounds
A quick learner with excellent listening skills
· Biotech and biopharma industry experience · Prior experience in business development, life science consulting, program leadership, and/or alliance management preferred · Financial modeling experience desirable · Candidates with various levels of experience will be considered and the job title of the new hire will depend on the qualifications and experiences of the successful candidate
operations manager
Working hours
full-time
Language
english
Responsibility
reporting to the Associate Director / Director of Clinical Operations, the Sr
study Manager will be accountable for planning, execution management and closure of clinical studies
ensure appropriate Clinical Operations input for studies prior to decision making
location: London or Boston
contributes to protocol development, including Clinical Operations feasibility assessments
reporting to: Associate Director/ Director of Clinical Operations
the Study Manager will accomplish this effort by working with the cross functional study team on day to day activites, both internally and with vendor teams to ensure the study is conducted according to the protocol and by following applicable guidance and regulations while meeting on time delivery of clinical milestones as established by business goals
responsible for clinical studies across phases 1 to 4, this person will be proactive in identifying study risks and leading problem solving efforts
Requirements
experience Required
strong expererience & knowledge of clinical project management in managing clinical studies from being to end
experience in oversight of external vendors
understanding of regulatory environment, GCP/ICH and compliance requirements for clinical research
experience working in an academic environment is a plus, as well as experience in rare disease areas and/or gene therapy
technician
Responsibility
conduct microbiology workflows for preparation of plasmids stocks and libraries
perform routine cloning to generate plasmid and Lentiviral Vector constructs
conduct cell culture and transfection workflows for the production of Lentiviral Vectors
determine titer and conduct quality control of viral particles using flow cytometry and droplet digital PCR methods
test and optimize protocols for production and quality control of viral particles
organize and track samples during production and storage
support lab operations, including inventory management, solution preparation, and standard lab tasks, including routine mycoplasma testing
contribute towards the preparation, review and completion of study reports and protocol SOPs
Requirements
candidates must have experience in cellular and molecular biology
skills required include mammalian cell culture, vector engineering, genetic engineering e.g. Cloning, PCR, transfection, transduction, and assay development
experience of working with Lentiviral Vectors
organised and proactive with the ability to manage multiple tasks efficiently and be flexible and adaptable as needed
strong interpersonal and communication skills to effectively collaborate with the research team and cross-functionally as necessary
keen attention to detail, with a good analytical ability to interpret data sets
ability to analyse and write up data, and to keep accurate records
candidates should also be highly motivated and eager to take responsibility for their part in the achievement of Orchard’s mission
clinical scientist
Language
english
Requirements
required Knowledge
accountable and responsible individual
excellent organizational skills
‘Can-do’ attitude and willingness to be flexible
able to manage complex data
curious and problem-solving mindset
experience in protocol writing, clinical trial activities, and clinical study report writing, ideally gained through roles such as Clinical Researcher, Clinical Research Associate , Clinical Trial Assistant , or Clinical Scientist
able to work in a dynamic environment
Education
life Sciences degree: BSc / Master’s Degree / PhD
Responsibility
contribute to the authoring and take responsibility for completing updates of clinical study documents
plan, review and support the deliverables related to clinical studies
ensure maintenance of the specific program folders