The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site per
The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site per
Spherion has a temp to hire opening for a Civil CADD Drafter in the Opelousas, LA area.This full-time, on-site role focuses on creating technical civil engineering plans?including bridges, roads, and general infrastructure, primarily using MicroStation. You will work side-by-side with project managers and engineers to build accurate construction submittals (alignments, profiles, quantity estimations) that meet Louisiana DOTD guidelines.Schedule: Full-time,
Spherion has a temp to hire opening for a Civil CADD Drafter in the Opelousas, LA area.This full-time, on-site role focuses on creating technical civil engineering plans?including bridges, roads, and general infrastructure, primarily using MicroStation. You will work side-by-side with project managers and engineers to build accurate construction submittals (alignments, profiles, quantity estimations) that meet Louisiana DOTD guidelines.Schedule: Full-time,
We are seeking a detail-oriented Logistics Planner for a full-time, temp-to-hire opportunity. In this role, you will oversee invoice processing, tracking, and reconciliation within a fast-paced logistics environment. The ideal candidate blends strong business or accounting fundamentals with sharp problem-solving capabilities to ensure accurate financial data management and smooth vendor communications.Responsibilities:Collect, receive, and manage files and
We are seeking a detail-oriented Logistics Planner for a full-time, temp-to-hire opportunity. In this role, you will oversee invoice processing, tracking, and reconciliation within a fast-paced logistics environment. The ideal candidate blends strong business or accounting fundamentals with sharp problem-solving capabilities to ensure accurate financial data management and smooth vendor communications.Responsibilities:Collect, receive, and manage files and
We are seeking a detail-oriented and customer-focused Order Entry Clerk to join our team. In this role, you will be responsible for processing incoming customer orders, scheduling deliveries, and providing top-notch customer support. The ideal candidate has prior experience in data entry or a call center environment, possesses strong Microsoft Excel skills, and thrives in a fast-paced setting where accuracy and professionalism matter.Responsibilities:Order
We are seeking a detail-oriented and customer-focused Order Entry Clerk to join our team. In this role, you will be responsible for processing incoming customer orders, scheduling deliveries, and providing top-notch customer support. The ideal candidate has prior experience in data entry or a call center environment, possesses strong Microsoft Excel skills, and thrives in a fast-paced setting where accuracy and professionalism matter.Responsibilities:Order
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, c
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, c
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