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

PROGRAMMING:

• Program and QC datasets and TFLs following specifications and good programming practice.
• Develop dataset specifications that conform to CDISC data standards.
• Attend and contribute to internal and client study team meetings.
• Mentor less experienced members of the team.

DAILY INTERACTIONS:

•  Communicate directly with other study team members and client key contacts.
• Share updates on ongoing work internally and at client meetings.
• Collaborate with the internal Veramed team to deliver high quality work on time and to budget.
• Contribute programming expertise and wider industry knowledge as required.
• Provide support and mentoring for more inexperienced members on the team.

OPPORTUNITIES FOR: 

• Development into lead programmer or technical role.
• Gaining experience across different therapeutic areas and phases.
• Presenting at conferences.
• Peer mentoring and/or line management.
• Developing innovative solutions to aid study reporting.
• 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.

BENEFICIAL EXPERIENCE:

• Understanding of the clinical drug development process and relevant disease areas.
• Awareness of industry and project standards as well as ICH guidelines.
• Proficiency in using SAS or other statistical software (e.g. R) appropriate to the level of seniority.
• A good understanding of CDISC data standards.
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables.
• 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.

Please Note: for a Programmer II to fully operate as Technical Programmer, we require at least 3 years of relevant industry experience.

Do you have an aptitude for developing technical solutions and an appetite for innovation? This role might be for you!

We are seeking a Programmer with a flair for computing environments and programming languages or deep knowledge of technical data standards. Should have an aptitude for developing technical solutions and advising team members and stakeholders, with an appetite for innovation.

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.

PROGRAMMING:

• Support the specification, development, validation, delivery and adoption of SAS & R tools and techniques following the software development lifecycle (SDLC) as applied to clinical trials.
• Provide technical expertise to support the delivery teams.
• Validation and oversight of biostatistics platforms and tools and the creation and maintenance of associated documentation.

DAILY INTERACTIONS:

• Act as the subject matter expert (SME) in the business, providing technical insight and consultancy.
• Share technical and wider industry knowledge (including clinical trial, therapeutic area and scientific context) with the client study teams and internal colleagues.

OPPORTUNITIES FOR: 

• Presenting at conferences.
• Contributing to business process improvements and authoring/presenting internal training.
• Providing significant contribution to internal Hackathons.
• Contributing to initiatives that consider employees, the environment and our local communities as part of our B Corp accreditation.
• Maximising knowledge sharing across the industry.

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.

BENEFICIAL EXPERIENCE:

• Excellent verbal and written communication skills with the ability to vary style and level and adapt to different working styles to understand needs of stakeholders.
• Completer-finisher abilities with a high attention to detail.
• Ability to translate strategy and elicited needs into practical project implementation and delivery.
• Understanding of data standards conformance and compliance.
• Excellent problem solving abilities.

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.

Act as Lead Programmer for one or more studies, taking responsibility for leading the programmers to ensure a successful delivery.

We are seeking a Programmer with leadership and organisational skills to work as part of the statistical and programming team providing programming support as outlined below to a variety of clients in the Veramed portfolio. This role provides the opportunity to progress towards becoming a Portfolio Lead Programmer 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.

PROGRAMMING:

• Act as lead programmer for client projects and studies.
• Contribute to the maintenance of the project plan.
• Proactively manage programming resource task assignments, scope change and risks.
• Contribute to the management of the delivery of projects within budget.
• Manage client expectations and issue resolution.

DAILY INTERACTIONS:

• Build an effective and collaborative relationship with the client.
• Lead the internal Veramed programming team to deliver on time, within budget, high quality work.
• Provide support and mentoring for more inexperienced programmers on the team.

OPPORTUNITIES FOR: 

• Potential to develop into Portfolio Lead role.
• Contributing to initiatives that consider employees, the environment and our local communities as part of our B Corp accreditation.
• Peer mentoring and/or line management.
• Taking ownership of a study or group of studies and implementing new ideas and processes to aid delivery.

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.

BENEFICIAL EXPERIENCE:

• Understanding of the clinical drug development process and relevant disease areas.
• Awareness of industry and project standards as well as ICH guidelines.
• Experienced in the implementation of data standards at a study level.
• Interpersonal/teamwork and communications skills for effective interactions.
• Proficiency in using SAS or other statistical software (e.g. R).
• Team leadership skills with a focus on results for timely and accurate completion of competing deliverables.
• Demonstrated problem solving ability and attention to detail.

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.