Senior Manager, Feasibility - REMOTE, USA
Deerfield, IL
Ability to evaluate the intent of the study concept and make informed recommendations based on scientific review and information available at the time of the request Ability to effective...

Director, Clinical Research Scientist - REMOTE, USA
Deerfield, IL
Development of protocols for clinical studies. Preparation of clinical development plans. Drafting of clinical scientific documents such as IND, IND amendments, Investigator Brochures, A...

Manager, Clinical Outsourcing - REMOTE, USA
Deerfield, IL
Assist Associate Director and senior leadership in the management of the Phase I Clinical Development outsourcing, vendor selection and clinical contracts process Generate RFIs, RFPs, an...

Manager, Clinical Compliance - REMOTE, USA
Deerfield, IL
Provide quality leadership and direction to Sponsor's R&D stakeholders on GCP related activities/issues and act as GCP expert/consultant for R&D colleagues. Act as a Clinical Compliance...

Trial Master File Specialist - REMOTE, USA
Deerfield, IL
Perform Quality control activities process for TMF submissions to Veeva Vault (VV) eTMF in accordance with the documented process Carry out required activities in VV eTMF for all Clinica...

Site Contracts and Grants Manager - REMOTE, USA
Deerfield, IL
Under the direction and as requested by the the sponsor CPMs, the Contracts and Grants Manager may Assists with the development of Investigator/Institution contracts and site budgets Pro...

Director, Clinical Pharmacology - Wilmington, DE
Wilmington, DE
Providing strategic leadership and demonstrating accountability for the clinical pharmacology programs supporting Phase 1 4 clinical development for development compounds Representing th...

Senior Manager, Site Start Up - REMOTE, USA
Deerfield, IL
Trial Start Up Group Accountable for advancing study start up activities for outsourced trials by understanding the objectives and assisting in the review and approval of the plan for co...

Senior Medical Writer
Cambridge, MA
Our client is seeking an experienced Medical Writer (MW) to lead and drive the writing of clinical and regulatory documents across the client's portfolio. The Medical Writer will closely...

Research and Development Associate
Cambridge, MA
Execute surface plasmon resonance (SPR) analysis for small molecules binding to protein and/or protein interactions. Work both independently and as part of a team to ensure project team...

Director, Clinical Scientist
Philadelphia, PA
Develops scientific understanding of assigned program and protocol requirements Supports protocol design and development strategy for clinical trials Manages protocol development process...

Senior SAS Programmer
Woodcliff Lake, NJ
Lead the development and implementation of submission ready SDTM datasets in accordance with regulatory requirements (e.g., FDA, EMA, PMDA). Collaborate with regulatory affairs and quali...

Senior Sales Specialist
Northfield, IL
Drive sales pipeline for Endoscope Repair and full repair catalog. Grow and retain existing accounts by presenting new solutions, products and services. Prepare and or participate in lar...

Senior Clinical Research Associate
Minneapolis, MN
The Sr. CRA is responsible for assisting with the execution of high quality clinical studies and will focus on the oversight and monitoring of investigational sites to ensure compliance...

Manager, Business Development
Deerfield, IL
Follow Standard Operating Procedures (SOPs) Maintain long term client relationships resulting in the expansion of client base. Directly implement initiatives to help build awareness of o...