Why consider joining us? As a member of our thriving team, you have the opportunity to work alongside clinical research colleagues who understand the patients’ mindset and their disease experiences. We help translate science into success for trials with a strategic and targeted, patient-centric approach. We are specialists who find solutions for novel trial challenges in our detailed approach throughout every study phase. From the beginning, we have nurtured an employee-centric company culture that focuses on patients’ needs. Precision’s team-focused culture ensures that team members will thrive and learn. These important key elements result in high quality work output while still having fun and giving back to the patient community.
Want to do a good job, help others and have a passion for making a difference.
Care about patients and understand the importance of quality data leading to successful outcomes.
Are highly experienced in clinical data management and have keen attention to detail, clear communication abilities and organizational skills.
Foster and value client and internal team collaboration.
Have a strong belief that all team members are valuable and appreciated.
Enjoy working alongside teammates and having project-specific data management and managerial support.
Excited about exercising your data management knowledge and expertise.
Look forward to opportunities to be involved in innovative data management technology initiatives and training.
A glimpse into the day to day:
Lead all aspects of the clinical trial data management process from pre-study start up to post database lock for assigned projects.
Collaborate with clients and team members to develop Case Report Forms (CRFs) and methodical data cleaning strategies to support protocol endpoints.
Be involved in the Electronic Data Capture (EDC) clinical database development and user acceptance testing (UAT).
Actively cleaning data, managing CRF and query trends and data reporting to ensure a clean database lock ready for analysis.
Work alongside key functional areas (such as Project Management, Biostatistics, Medical, Clinical, Safety, Quality Assurance, etc.).
Standard Operating Procedures / Work Flow Tools (SOPs/WFTs); regulatory directives; study specific plans and guidelines will be followed.
Minimum Required: Bachelor’s degree or in country local equivalent or equivalent related experience
Minimum 5 years of Clinical Data Management experience utilizing various clinical database management systems
Broad knowledge of drug, device and/or biologic development and effective data management practices
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Professional use of the English language; both written and oral
Experience in a clinical, scientific or healthcare discipline. Understanding of CDISC standards (CDASH, SDTM, etc.).
Academic concentration in one or more of the following, or related discipline; life sciences, computer science, or engineering.
Advanced degree in clinical data management, health informatics, biometrics or similar.
Precision medicine is revolutionizing the attack on cancer and rare diseases—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.
Reasonable estimate of the current range
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.