Study Director I

3 weeks ago

Westminster, United States CareerBuilder Full time

The position has responsibilities centered around the execution, planning,and management of assigned studies. The ability to communicate succinctly withclients, coordinators, and technicians is key as well as across-functional, flexible, and collaborative spirit. The successfulcandidate will have direct knowledge of the time and costs associated with agiven amount of scientific work, can communicate their scientific expertiseto key stakeholders of client companies, and can successfully executemultiple, concurrent studies in a timely fashion that matches businessdemand. The right candidate will help manage client projects to ensure theymeet client expectations and deadlines along with assisting with businessdevelopment activities. The position also requires astute attention todetail, demonstrable organization skills, and willingness to fully alignwith established company SOPs and best practices. The position demands anin-depth understand and working knowledge of translatable pre-clinical drugdiscovery and development with a focus on renal and/or pulmonary therapeuticar
Responsibilities
Participates in in vivo pharmacology research conducting biochemical screeningmodels, proof-of-concept models for target validation, as well as diseaseefficacy models to evaluate development and discovery lead compounds.Participates in pharmacology study organization, layout, and executionwith excellence and limited supervision.Extensive handling of research rodents including administration (e.g.,p.o., i.p., s.c., i.v.) of test and/or challenging agents, bloodcollection (e.g., direct cardiac puncture, tail bleed,retro-orbital), and necrParticipates in physiological functional testing including, but not limitedto, indirect and direct systemic hemodynamics, renal function, andpulmonary function.Participates in survival surgery of research rodents.Acts as a liaison between external clients/sponsors and the in vivotechnical team.Owns and provides leadership for all aspects of the appropriate protocolprocess (text, quote, and/or response to requests for information)for assigned opportunities, inclusive of managing opportunitiesautonomously, establishing clear timelines, meeting client requirements,and resolving obstacles.Reviews and analyzes client inquiries and documents to ensure adequateinformation for quote and protocol preparation is provided. Follows up withappropriate contact for additional information as required.Identifies and resolves issues around client's requirements and thecompany's capabilities.Perform in-depth analysis of client issues in order to remediate or preventclient dissatisfaction and develop and maintain customized clientcommunication.Keep track of project timelines for forecasting purposes.Prepares high quality and accurate data package for clients.Oversees and participates in final Technical Report writing.Identifies and is accountable for driving ways to improve the efficiency andquality of processes and the resulting deliverables, influencing keystakeholders as applicableAdheres to company standards, research SOPs and required safety procedures.Other duties as assigned.
Qualifications
A basic understanding of integrated physiology, pathophysiology, andpharmacology is required.Previous pre-clinical in vivo laboratory experience including handling ofresearch rodents is required.Industry research experience is highly preferred.Research experience in renal and/or pulmonary therapeutic area is highlypreferred.Ph.D. degree in related scientific discipline (e.g., Physiology,Pharmacology) is highly preferred.MS degree in related scientific discipline (e.g., Physiology,Pharmacology) and at least 3-8 years of related experience or an equivalentcomb nation of education and experience is required.An individual with an in-depth understanding of in vivo models of multi-systemrodent physiology and in vitro analyses of pathobiology and diseasebiomarkers.Demonstrates strong organizational, communication (both oral andwritten), time management, and interpersonal skills in across-functional team.Must actively participate and work well in a collaborative, team-orientedenvironment.Experience with rodent survival surgeries is desired.Should be adept at data management and reduction.Able to demonstrate strong skills in authoring and managing the production ofscientific documents (e.g., pre-clinical study protocols, datapackage, technical reports, publications in peer-reviewed journals).Proficient with Microsoft Excel, Word, and PowerPoint; familiarity withGraphPad Prism desired.

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