Job description: 4449 Posted: 22/12/2023

• Competitive
• Home Based , United Kingdom
• Permanent

Senior Statistical Programmer II – FSP | Leading CRO | UK | Home Based |

Industry leading CRO who are on a mission to improve health have a new opportunity for a Senor Statistical Programmer II to join them in the UK or across Europe. This is a fantastic opportunity to join an organisation with a truly collaborative and winning culture with a focus on flexible working and work-life balance. This is an urgent opportunity for an experienced Statistical Programmer II looking for a mix of hands-on technical programming and study lead.

As a Senior II/Principal Programmer with FSP, you will act as the lead programmer, project lead, or project oversight lead, dedicated to one client and overseeing the statistical and bioinformatics programming aspects of clinical trials from design through analysis and reporting.

What you will be doing:

• Act as the lead programmer or project lead on studies of significant complexity.
• Work directly with project team leaders and client representatives to conduct team meetings, develop and maintain project timelines, assess and forecast resources, and monitor study budgets.
• Assume leadership responsibility as a contributing member of a multidisciplinary project team, communicating actively and frequently with other team members and ensuring adherence to working practice documents and SOPs.
• Independently create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems, combine data from a variety of sources and structures, generates and store summary data from a variety of sources, generate reports or combines multiple databases and validates programs that generate listings, tables and figures using SAS.
• Manage and document assignments to meet timelines and deliver high quality work, being familiar with any relevant contractual obligations or limits.
• Increase knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry.
• Provide training, guidance, and project leadership to junior team members.
• Provides input into bidding process as requested.

What you will need:

• Bachelor’s degree or equivalent in computer science, mathematics, statistics, data science/analytics, or other relevant scientific and at least 8 years’ experience in hands-on programming, with lead programming experience.
• ADaM, TLF programming, DMC support and regulatory support experience.
• Proven experience as an independent, lead programmer.
• Experience programming complex analysis datasets and outputs (efficacy, complex lab and regulatory requests).
• eCRT and define.xml knowledge.
• Strong written and verbal communications skills to effectively interface with teams and clients globally, including proficiency in the English language.
• Demonstrated leadership ability and ability to work on a multi-disciplinary project team, training, and mentoring others.
• Capable of providing quality control review for statistical programming and identifying solutions and process improvements.
• Able to independently and effectively organise and manage multiple assignments with challenging timelines.
• Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with others.

What’s in it for you:

• Work for a global organisation with a local feel who are dedicated to supporting and fostering work-life balance and flexibility.
• Access to award winning learning and development program ensuring you reach your full potential.
• Fully home based with all equipment provided.
• Very competitive salary plus extensive benefits package based around employee’s health and well-being.
• 10% annual performance-related bonus.
• Immediate interviews available.

What to do next:
If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the Senior Statistical Programmer II onboard as soon as possible.

Not what you’re looking for?
Please contact Jo Fornaciari on 0330 335 9476 for a confidential discussion about potential opportunities.

Expected salary:

Location: United Kingdom

Job date: Fri, 22 Dec 2023 23:17:18 GMT

Apply for the job now!

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Job description: Updated: Yesterday

Location: North America-United States, United States

Job ID: 23006899-USA

Description

Senior Statistical Programmer – FSP model

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job responsibilities

• Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.
• Works to ensure that outputs meet quality standards and project requirements.
• Performs validation programming and works with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
• Keeps project team members informed of programming progress and issues requiring their attention.
• Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).
• Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.
• Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.
• Develops specifications for datasets and outputs of any complexity according to statistical and sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework.
• Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
• Conducts effective internal meetings (appropriate in format, frequency and attendance). Distributes relevant information in advance. Ensures minutes are promptly and accurately distributed. Follows action items through to completion, and maintains order and focus of meetings, working toward consensus.
• Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
• Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and statistical programming management, and completes project programming activities within timeframe allotted.
• Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables.
• Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design. Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.
• Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor.
• Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process.
• Transfers deliverables.
• Performs other work-related duties as assigned.
• Minimal travel may be required

Qualifications

What we’re looking for

• Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience.
• Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
• Excellent written and verbal communication skills.
• Ability to read, write, speak and understand English.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about .

Additional Information:

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

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Expected salary:

Location: USA

Job date: Sat, 11 Nov 2023 02:20:38 GMT

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