Work on a range of clinical studies for small to large pharmaceutical and biotech clients while feeling valued and supported in your day-to-day work. 

We are seeking  a hands on  Statistician with attention to detail and strong work ethic to work as part of the statistical and programming team providing statistical support as outlined below to a variety of clients in the Veramed portfolio. This role provides the opportunity to progress towards becoming a Lead Statistician at Veramed.

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 you have a passion for contributing to high quality deliverables, thrive when working closely with team members of all levels of experience and want to work for a company where you truly feel you can add value, this role could be for you. Apply now.