Clinical Data Analyst (Us)

CluePoints is an innovative, fast-growing company and the premier provider of Risk-Based Monitoring and Data Quality Oversight solutions to clinical research organizations. Our products enable both risk planning and operational risk monitoring, and utilize advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution. CluePoints is seeking outstanding candidates with strong data analytics aptitude and a passion for delivery excellence, to help drive customer success and broad adoption of the CluePoints solution.

Please apply only if you hold a valid work permit or if you are a national of the Member States of the European Economic Area.

Responsibilities

• Ensure that appropriate documentation is produced and maintained for each study
• Summarize findings and support the communication of results to customers (both written report and oral presentation)
• Perform analyses using the CluePoints Central Monitoring Platform – diagnosing and explaining anomalies identified in the clinical study data
• Assist Business Development and Quality Assurance teams in responding to client questions and requests (e.g., RFP responses, audits, etc.)
• Provide consultation and related operational support to customers as needed, with the help of more senior Data Analysts and/or the CluePoints Project Manager as well as mentoring more junior Data Analysts as needed
• Participate in the continuous improvement and development of our product solutions and operational processes
• Perform the technical configuration of the CluePoints solution for clinical studies based on customer requirements

Skills Needed

• High degree of accuracy and attention to detail
• Experience with CDISC databases is a plus
• Aptitude for mathematical and statistical concepts and data analytics
• Experience with and understanding of clinical trials and clinical data
• Experience in delivery of technical solution trainings is a plus
• Experience with one or more programming languages, including SAS
• Ability to thrive in a fast-moving environment, under time and resource constraints
• Excellent oral and written communication skills in English
• Experience and ability to work well in a team environment

Qualifications Needed

• Knowledge of industry regulatory and clinical data standards including 21 CFR Part 11, ICH E6 (GCP), CDISC standards, MedDRA, WHODRUG, etc.
• College degree, preferably in a scientific or technical discipline
• +2 years of experience in a clinical research environment

Top Reasons to Work with Us

• At CluePoints, learning, training and personal growth are part of the game: you’ll have access to online training materials, certifications sponsored by the company, personal growth plans, and career paths to explore new opportunities.
• Last but not least, we offer competitive salary and benefits, bonus potential, employee referral program.
• Please simply click the button on this page!
• Hybrid with possibility of remote (dependent on roles and responsibilities)
• Many activities are organized during the year such as team lunches, happy hours, team buildings, holiday parties and many other celebrations!
• Flexibility is part of our DNA
• Our offices provide a fun atmosphere: PS4, foosball, and our newly added dartboard
• You’ll have a challenging and rewarding job in an ambitious and fast-paced technology scale-up that has received many national and international awards including “Scale-Up of the year 2019”!
• You’ll work with a fast-growing, multi-disciplinary and international team representing over 20 different nationalities, in an English-speaking working environment.