As part of the local TMF team, the LTRS will: • Follow Sponsor’s training, instructions, and reference documents for accurate filing of trial documents into Sponsor’s TMF • Manage the workload for assigned trials (approx. 5-7) • Work with the Clinical Trial Manager and trial team to identify and maintain the country and site specific List of Expected Records (LoER) • Perform quality checks on filed documents according to current standards and instructions • Track filing activities and quality checking results using Sponsor’s provided tools and i...

Site engagement is a critical component in the execution of a clinical trial. Engagement of highly motivated clinical investigators will enable UCB to maximize efficient and timely delivery of UCB’s clinical trials. This position is responsible for contributing to an industry leading site engagement team. The Site Engagement Manager is responsible for providing operational expertise to sites through ownership/management of Site Engagement Strategy. The scope of this role includes the following: • Define and implement strategies for engaging clinic...

Our client, a nationally acclaimed interdisciplinary research center seeks Java - Spring software development professionals. Title: Sr Software Developer (early/mid career) Location: Northern Mississippi. Multi-cultural, progressive university community offering a low cost of living with all the amenities. Minimal traffic - commutes. Company: • A nationally acclaimed interdisciplinary research center Experience Profile: • Bachelors with 3+ years experience devoted to Java programming. • Hands-on Java web application development using...

Responsibilities • Manages and tracks investigational product (IP) inventory; advises supply management team of potential shortages and makes recommendations for resupply activities based on usage trends. • Initiates IP shipment orders according to supply plans or as requested by Clinical Trial Management team; tracks orders through receipt at investigator study sites; communicates with distribution vendors to ensure timely and compliant shipment and delivery to investigator sites. • Reviews and evaluates temperature excursion data and communica...

Responsible for managing data management teams, studies and programs of studies under the general direction of Sr. Project Manager or the Director of Data Management. • Work with Clinical Operations, CDMS, Biostatistics, CDS, ITG, Medical Writing, Regulatory Affairs and Quality Assurance to ensure that data collected during trials are managed according to corporate standards and meet regulatory guide lines for data integrity.

Our client is currently hiring! MID WEST, WEST COAST and EAST COAST positions available. Home based CRA opportunities with a successful, global CRO. Regionalized, lower travel. Excellent Compensation and sign on bonus currently available. Please email for details!

Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts. Principal Responsibilities: Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical tr...

Job Title: Clinical Research Associate Experience: 3+ years Therapeutic areas:Oncology Location: Canada Roles & Responsibilities of the position PRINCIPAL RESPONSIBILITIES: - Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team - Acts as primary local company contact for assigned sites for specific trials. - Attends/participates in investigator meetings as needed. - Responsible for executing activities...