Veeva API help

Veeva API help

Help required- someone who is very knowledgeable of Veeva APIs.  This is probably not a large project, maybe just a couple of hours, but could lead to more.  Here is the description of the business problem: we’ve been creating some forms for quick creation of Veeva objects, and that’s working fine… but I’m looking for […]

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TransCelerate Common Technical Protocol integration into Starting Point Templates

TransCelerate Common Technical Protocol integration into Starting Point Templates

Mid sized Northeast US based drug sponsor‘s goal is to update our StartingPoint authoring templates (SP) and incorporate relevant aspects of TransCelerate’s (TCB) Common.  Tasks include conducting a Comparison of our current SP templates with TCB’s CPT, identify differences between TCB CPT from current templates; collect feedback from current users within the core team., execute updates to […]

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Patient Data Compliance and Governance needed for De-Identified Data project

Patient Data Compliance and Governance needed for De-Identified Data project

Emerging patient data technology start up in need of an independent expert on patient data privacy.  Company intends to ingest de-identified data from partner healthcare providers in the US, Germany, UK, France, Spain and Italy on an ongoing basis.  End goal is to simulate, as close as possible to true patient data without violating privacy […]

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Manager, Technical Services

Manager, Technical Services

Small anti-infectives, US based (northeast) drug sponsor to conduct 2 studies to support a new drug application. Study start up, first patient in target- end of Q1 2022.  Primary Responsibilities  The primary responsibilities of this role include but are not limited to: Management and oversight of all technical and building-related operations and services, including responsibility […]

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Veeva RIM Vault and Regulatory Operations Consulting

Veeva RIM Vault and Regulatory Operations Consulting

Small CA based biotech in need of an independent expert who knows both Veeva (any vault) AND regops.  “What we’re finding is that people either know one or the other.  We need both!” Number of hours and duration, not sure, it really depends on the expertise of the consultant.  Deep understanding of the regops process, […]

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Q-Sub- AI

Q-Sub- AI

Independent consulting experience needed writing/reviewing Q-Sub/Pre-Sub for a device. Product: This is an AI platform which functions as a risk assessment tool for maternal hemorrhage. Timeline: Project would commence In August 2022 and extend over the next ~45days.

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Document Formatting (and possibly templates) Expertise Needed- Large Pharma Module 4 Group

Document Formatting (and possibly templates) Expertise Needed- Large Pharma Module 4 Group

Large US hub for one of either Astellas/Takeda/Daiichi Sankyo/Chugai (need mutual NDA in place for LifeSciHub to disclose). Non Clinical Writing and Submissions group within Preclinical and Translational Sciences needs document formatting support for any and all potential content:  study reports, publications, submissions, etc. Hours and duration- to be determined.  At present the need is […]

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Pharmacovigilance Program Manager- Safety System Data Migration

Large, UK based CRO in need of a contract PM to facilitate a migration of data from one PV system onto the Oracle Cloud.  Strong project management required, pharmacovigilance domain expertise also required, familiarity with Oracle Argus, both in-house as well as cloud.  Project expects 20 hours a week for 6 months.  Must be able […]

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