Precision Medicine Group
Principal Clinical Data Scientist
Remote role where the employee must remain based in a particular country.
Mexico only
Employer listed it 2 days ago · Added today
First listed 2 days ago.
Salary
Not stated
Location
Mexico only
Timezone
Not stated
Contract
Full-time
Experience
Lead
Category
Data
This employer didn't state pay. Jobs like this usually pay around $185k–$265k a year, a typical range taken from 158 lead-level data roles on Nomaders that do state pay. It's a guide, not an offer.
Remote flexibility
Work from home
This is a remote role, but the employee must be based in Mexico. It is work from home rather than work from anywhere.
What the employer says
- Source listing states candidate location: "Remote, Mexico, Remote (Mexico)"
What Nomaders makes of it
- Residency required in Mexico
- Payroll and tax are likely handled in that country only
The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.
About the role
Position Summary:
The Principal Clinical Scientist, Clinical Science Analytics & Insights is responsible for & manages the operational clinical science function from study start up through database lock for assigned projects focused on the scientific & indication specific insights into data collection & data visualization outputs to support scientific, clinical-sense data cleaning as part of Precision’s cross-functional data review team. Serves as the subject matter expert in the application of clinical knowledge, guidelines & standards of care to the review of clinical trial data. Serves & contributes to project teams as the CSAI functional lead delivering within scope, time & cost.
Essential functions of the job include but are not limited to:
Serve as the functional lead implementing CSAI services per study scope of work (SOW) on assigned project team(s)
Serve as a resource for project teams regarding scientific related data capture, review & cleaning.
Support & participate in the development & implementation of process flow for integrated, cross[1]functional, data cleaning for interim &/or final study data deliverables between all applicable departments (e.g., data management, medical, safety, vendors, sponsor, etc.)
May be responsible to cross-functionally manage the overall data cleaning process internally to support interim &/or final data deliverables (e.g., tier cleaning process/timelines, etc.)
Manage Medical Monitor review of subject data.
Provide protocol review from a scientific operational perspective.
Provide indication-focused, scientific, clinical input & support to Data Management in the development & revision of eCRF specifications, edit checks & completion guidelines &/or other study[1]specific documentation as applicable.
Provide indication-focused, scientific, clinical input & support to Data Management in the conduct of EDC UAT supporting the CSAI function as applicable.
Collaborate to support cross-functional departmental communication including internal CSAI communication as applicable on data capture, review trends, EDC updates, CSAI Programming needs, etc.
Support the identification of study risks including the management to correct any CSAI study-specific deficiencies.
Support Project & Financial Management on monthly invoicing & variance management of the CSAI budget
Collaborate with CSAI management to ensure that CSAI resource needs are adequately addressed due to scope of work changes.
Oversee &/or develop & maintain CSAI project related plans, guidelines, & trackers
Ensure applicable eTMF documentation related to CSAI is maintained as per study project plans & SOPs.
Support &/or conduct holistic &/or aggregate scientific, clinical sense data review based on defined manual Clinical Data Review Guidelines using various programmed outputs including but not limited to Smart Patient Profiles™, Smart All-Patient-Data Workbook, listings, quality metrics &/or graphs.
Oversee &/or issue & resole queries in various EDC systems.
Review &/or provide routine status updates on CSAI data review findings & escalate issues as appropriate.
Manage &/or conduct the development & associated User Acceptance Testing (UAT) of CSAI programmed output(s)
Provide study-specific training for CSAI Scientists, project teams &/or study sites based on review findings.
Participate in internal & external study-specific team meetings &/or presentations as applicable including facilitating CSAI meetings or topics.
May support study-specific data related committees &/or meetings (e.g., safety review committee)
Requirements
- ·Minimum Required:
- ·Bachelor’s degree or equivalent combination of education/experience in science or health-related discipline with proficiency in medical terminology
- ·Minimum of 8 years of clinical research experience or proven competencies for this position
- ·Minimum of 1 year of leadership experience
Benefits
No benefits package published with this listing. Ask about it at first interview.
How to apply
- 1Check the flexibility label above, work from home, matches where you plan to live and work.
- 2Tailor your CV to the role at Precision Medicine Group, mentioning your remote working experience.
- 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.
Found 12h ago. Last checked 23 Sept. Always confirm the details on the original posting, salary and location can change after publication.
Listing sourced from Company boards.
Similar roles
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Free to apply, no account needed.
Typically $185k to $265k per year · You'll be taken to the employer's careers page.