Business Integrator
other jobs Cpl Life Sciences
Added before 6 Days
- Wales,Wrexham
- full-time
- Salary negotiable
Job Description:
Role: Project Manager
Location: Wrexham working 4 days a month in the office
Pay Rate: £208 per day
Key Skills: strong technical writing skills and digital literacy
Position Summary
This role is a key support role within Aparito. You will support the team by completing a variety of tasks from day-to-day trial support of scientific tasks, completing compliance and validation documents and supporting the team in a fast-paced environment.
Duties and Responsibilities
Trial support
· Maintain trial organisation, keep records and reports up to date
· Supporting trial process and compliance
· Ensuring regulatory requirements and company policies are being followed with high attention to record documentation
· Support communications with external clients/partners
· Co-ordinating travel arrangements
· Planning and scheduling of meetings
· Supporting senior managers with clerical tasks
Scientific support
· Support writing and reviewing of study documents (protocol, statistical analysis plan, reports)
· Support drafting and coordinate submission of scientific publications, including posters and peer-reviewed articles.
· Support the team by coordinating the engagement with regulatory agencies (EMA, FDA) regarding qualification of novel eCOA/digital biomarkers.
· Support drafting of presentations and creation of figures and visuals, for both internal and external dissemination, according to company guidelines.
· Perform weekly and ad hoc literature searches of therapeutic areas of interest, digital health technologies and best practices and update the team on new developments.
· Keep abreast of updates on regulatory guidance concerning electronic data collection, digital biomarkers and outcome measurement and decentralized clinical trials.
Key Skills and Competencies
· Life-science graduate with research and/or project management experience in public or private sector
· Strong interest in digital health technologies applied to drug development, outcome measurement science and regulatory affairs.
· Proactive and creative; problem-solver and pragmatic, but with a broad vision to improve processes and share knowledge.
· Team player
· High digital proficiency
· Excellent verbal and written communication skills – especially technical writing
· Strong organisational and time-management skills
· Strong presentation and public-speaking skills
· Ability to collaborate with others
· Relevant experience of a similar role
Work Environment
Aparito is a high growth, tech company. The ability to be productive and successful in a fast-paced work environment is critical. If you are comfortable dealing with uncertainty and shifting priorities (with a supportive team alongside you), this role could be a good fit for you.
If you are interested, please send your CV to
Location: Wrexham working 4 days a month in the office
Pay Rate: £208 per day
Key Skills: strong technical writing skills and digital literacy
Position Summary
This role is a key support role within Aparito. You will support the team by completing a variety of tasks from day-to-day trial support of scientific tasks, completing compliance and validation documents and supporting the team in a fast-paced environment.
Duties and Responsibilities
Trial support
· Maintain trial organisation, keep records and reports up to date
· Supporting trial process and compliance
· Ensuring regulatory requirements and company policies are being followed with high attention to record documentation
· Support communications with external clients/partners
· Co-ordinating travel arrangements
· Planning and scheduling of meetings
· Supporting senior managers with clerical tasks
Scientific support
· Support writing and reviewing of study documents (protocol, statistical analysis plan, reports)
· Support drafting and coordinate submission of scientific publications, including posters and peer-reviewed articles.
· Support the team by coordinating the engagement with regulatory agencies (EMA, FDA) regarding qualification of novel eCOA/digital biomarkers.
· Support drafting of presentations and creation of figures and visuals, for both internal and external dissemination, according to company guidelines.
· Perform weekly and ad hoc literature searches of therapeutic areas of interest, digital health technologies and best practices and update the team on new developments.
· Keep abreast of updates on regulatory guidance concerning electronic data collection, digital biomarkers and outcome measurement and decentralized clinical trials.
Key Skills and Competencies
· Life-science graduate with research and/or project management experience in public or private sector
· Strong interest in digital health technologies applied to drug development, outcome measurement science and regulatory affairs.
· Proactive and creative; problem-solver and pragmatic, but with a broad vision to improve processes and share knowledge.
· Team player
· High digital proficiency
· Excellent verbal and written communication skills – especially technical writing
· Strong organisational and time-management skills
· Strong presentation and public-speaking skills
· Ability to collaborate with others
· Relevant experience of a similar role
Work Environment
Aparito is a high growth, tech company. The ability to be productive and successful in a fast-paced work environment is critical. If you are comfortable dealing with uncertainty and shifting priorities (with a supportive team alongside you), this role could be a good fit for you.
If you are interested, please send your CV to
Job number 1808045
metapel
Company Details:
Cpl Life Sciences
Company size: 50–99 employees
Industry: Scientific
CPL UK is a group of Specialist Talent businesses which service the Professional Services, Science, Technology, Engineering, Mathematics and Health se...