PSI CRO
More roles at PSI CROLead Data Manager for Clinical Trials
Remote role where the employee must remain based in a particular country.
Listed for Brazil
From the listing details: Source listing states candidate location: "São Paulo, SP, Brazil, São Paulo, SP, br, Remote"
Employer listed it 8 months ago · Added 2 weeks ago
Been open since 8 months ago. Long-running listings are sometimes left up after the role is filled.
Salary
Not stated
Location
Listed for Brazil
Timezone
Not stated
Contract
Full-time
Experience
Lead
Category
Data
The employer did not publish a salary, and we have too few comparable roles to estimate one.
What the advert says
Quoted word for word from the employer's advert. Where it says nothing, we say so.
- Working hours
- Not mentioned in the advert
- Where you can work from
- Location eligibility not confirmed
- Contract
- Not mentioned in the advert
- Experience asked for
At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable)
- Pay
- Not mentioned in the advert
Remote flexibility
Work from home
This is a remote role, but the employee must be based in Brazil. It is work from home rather than work from anywhere.
What the employer says
- Source listing states candidate location: "São Paulo, SP, Brazil, São Paulo, SP, br, Remote"
What Nomaders makes of it
- Residency required in Brazil
- 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.
Before you apply
Experience: employer states
Written as a requirement
- “College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities”
- “At least 3 years of experience of full scope of data management responsibilities in international EDC studies”
Written as a nice-to-have
- “Project data management experience is a plus”
Questions worth asking: Nomaders interpretation
- The advert does not say where you can be based. Ask which countries they can legally employ or contract you from.
- No pay is stated. Ask for the salary range before investing time in interviews.
- The advert does not say whether this is employment or a contractor arrangement. Ask, as it affects tax and benefits.
Produced automatically from this advert's text; not reviewed by a person. The employer's own page is the final word.
About the role
We’re over 2,700+ strong across the globe. We’re scientists, strategists, creatives, and innovators. We value individual brilliance and build a strong foundation for teamwork across all our business. We love the challenge of our industry. We’re changing lives and redefining success every step of the way.
The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision, or working under minimal supervision on data management activities for small to medium sized projects. 
 Communication
Primary communication point for project teams and company departments with regard to clinical data management
Communication line for clients/vendors for all data management aspects of clinical projects and clinical data management reporting
 Data Management
Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables. 
Primary responsibility for clinical data management activities within clinical projects, including, but not limited to: Study documents review
Data Management plan and other project-specific guidelines and instructions development and review
Co-ordinate/perform user acceptance testing
Development of Data Validation Plan/Edit Check Specifications
Data entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issues
Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding quality of data
Non-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding quality of data and other issues)
Database edits (paper CRF studies)
Manual CRF review (non-medical checks)
Clinical database lock
Coordination and supervision of processing, dispatch and archiving of CRFs/queries
Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol
Development of CRF completion guidelines
Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required)
SAE reconciliation
Electronic data transfer (import/export) specifications review and approval
Document Management
Requirements
- ·Advance your career in clinical research and develop new skillsets whilst growing with the organization.
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 PSI CRO, mentioning your remote working experience.
- 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.
Found 17d ago. Last checked today. Always confirm the details on the original posting, salary and location can change after publication.
Listing sourced from Company boards.
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