Manager Clinical Programming

MoonLake TX; Cambridge; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A dynamic biotech company in Cambridge is seeking a Manager to lead programming for clinical trials. You'll guide junior team members, ensure high-quality data outputs, and oversee external vendor programming activities. A degree in a related field and experience in SAS programming are essential. Join a company that values flexibility and offers career growth opportunities in a supportive environment.

Benefits

Learning environment

Impactful work

Career growth

Qualifications

• Experience in clinical trials and CDISC standards.
• Experience in leading programming teams.
• Highly organized and able to prioritize work.

Responsibilities

• Lead programming for clinical trials and manage internal programming activities.
• Mentor junior team members in clinical programming.
• Ensure compliance with company policies and procedures.

Skills

SAS programming

R programming

Clinical trial knowledge

Communication skills

Organizational skills

Problem-solving

Education

Degree in Computer Science, Mathematics, Statistics

Job description

Job Purpose

The Manager will lead and support the analysis and reporting of MoonLake sponsored clinical trials by directing and contributing to internal programming activities and the oversight of external programming activities to ensure high quality data, datasets and statistical outputs.

Your profile

Major Accountabilities

• Lead programmer for MoonLake sponsored clinical trials/indications, acting as primary Clinical Programming point of contact
• Provide guidance/mentorship to junior members of the Clinical Programming group
• For internal studies, lead and contribute to the specification, production and valida-tion of SDTM and ADaM datasets, Tables, Figures, and Listings (TFLs) in support of planned and exploratory analyses
• For outsourced studies, lead and perform oversight and review of vendor programming activities and deliverables
• Development of data review tools to support instream data review
• Effective and close collaboration with other Clinical functions (e.g. Medical & Drug Safety, Clinical Operations etc.)
• Ensure timely and accurate documentation of Clinical Programming activities (e.g. program headers, validation logs etc.)
• Maintain awareness of, and ensure compliance with, MoonLake policies and procedures

Job Requirements

• Degree in Computer Science, Mathematics, Statistics, or related disciplines
• Experience and understanding of clinical trials and CDISC standards
• Experience of SAS programming with experience of R programming being an advantage
• Experience of leading programming teams at the study and/or project level
• Good oral and written communication skills
• Highly organised, able to prioritise work and meet deadlines
• Independent, self-starter with a proactive, problem-solving approach

Why us?

An exciting job opportunity awaits you!

MoonLake is a dynamic and innovative company pushing the boundaries of possibility, and we are looking for passionate individuals to join our stellar team.

What we offer:

Learning Environment: An opportunity to learn and grow alongside experienced professionals in a supportive and innovative biotech environment.

Impactful Work: Contribute to ground-breaking projects that have the potential to transform global healthcare.

Flexibility and Balance: Work remotely/hybrid, enjoying a healthy work-life balance while making meaningful contributions to our team.

Career Growth: A clear path for career progression, with the chance to take on more responsibilities as you develop your skills.