top 3 scores:
Culture
Location flexibility
Inclusion
Job Description
KEY RESPONSIBILITIES:
This role entails a wide variety of responsibilities and client exposure – you are certainly not pigeon holed.
Below is a range of the types of tasks you could be carrying out on a daily basis. As with many roles at Veramed, you have the opportunity to shape their direction dependent on client needs and your own career aspirations.
STATISTICS & PROGRAMMING:
- Prepare and review study documentation including protocols, SAPs, TFL shells and analysis dataset specifications
- Input into choice of appropriate statistical methodology
- Manipulate, summarise and analyse clinical trial data using a variety of statistical techniques
- Program/validate statistical tables
- Mentor more junior members of the team
- Participate in internal and client meetings
OPPORTUNITIES FOR:
- Development to Lead Statistician
- Gaining experience across a range of therapeutic areas and/or phases
- Presenting at conferences.
- Developing and executing innovative study design and/or efficiency optimisation ideas.
- Peer mentoring and/or line management.
- Contributing to business process improvements and authoring/presenting internal training.
- Contributing to initiatives that consider employees, the environment and our local communities as part of our B Corp accreditation.
WHAT TO EXPECT:
- A warm, friendly working environment in which to thrive both personally and professionally.
- A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
- Exposure to a wide range of clients and projects, allowing you to diversify your workload and work closely with some of the biggest pharma companies in the industry.
- Work with a truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry.
- The ability to truly own your role and develop your skills and experience.
ADDITIONAL REQUIREMENTS:
- Understanding of clinical drug development process, relevant disease areas, endpoints and different study designs.
- Awareness of industry and project standards & ICH guidelines.
- Excellent verbal and written communication skills.
- Interpersonal/teamwork skills for effective interactions.
- Proficiency in data handling using SAS or other statistical software (e.g. R).
- Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
- Demonstrated problem solving ability and attention to detail.
- Ability to work independently and as part of a team.
If this role sounds right for you, please click 'apply now' to submit your application. We'd love to hear from you!
As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.
Company benefits
We asked employees of Veramed what it's like to work there, and this is what they told us.
Additional employee ratings
(these do not contribute to the FlexScore®)
Working at Veramed
Company employees
Gender diversity (male:female)
Funding levels
Currently Hiring Countries
India
Ukraine
United Kingdom
United States
Office Locations