We use cookies. Find out more about it here. Some services may not be available without accepting cookies. By continuing to browse this site you agree to our use of cookies.

I agree and accept cookies

Director, Site Management and Monitoring (SMM) Breast/Gyn job in Wilmington

Job Type

Location

Salary

Date posted

Job title

Vacancy has expired

Back to search results

Wilmington, Delaware - DE AstraZeneca

Job Ref:	R-241569
Employer:	AstraZeneca
Category:	Content Marketing
Job Type:	Full Time
Salary and Benefits:	USD 162,000.00 - 243,000.00 per year
Location
State:	Delaware - DE
City:	Wilmington
Post Code:	19803
Map:	United States, Delaware , Wilmington (Show on map)
Description
The Director, Site Management & Monitoring (DSMM) delivers the committed part of all clinical interventional studies under their management. This delivery must accord to agreed resources, budget, and timelines, and must comply with AZ Procedural Documents, international guidelines such as ICHGCP, and local regulations. The DSMM is responsible for line managing dedicated group(s) of staff and responsible for planning and use of staff resources, assigned budget, objective setting and performance follow-up. The DSMM is also expected to contribute to regional and or global tasks and initiatives as delegated. As assigned, the DSMM ensures that study sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. In some countries a DSMM may also take responsibilities as Local Study Associate Director (LSAD) or Clinical Quality Associate Director (CQAD) if required and agreed with the (Senior) Director, Country Head. You Will: Support SMM region in programs/activities as agreed with (Senior) Director, Country Head. Ensure collaboration with local Medical Affairs team. Ensure that study activities at country level comply with local policies and code of ethics. Review SQV reports of direct reports following AZ SOPs Review accompanied site visits/co- monitoring visits/training visits/QC visits performed to direct reports following the local QC plans. Perform accompanied site visits according to local QC Plan, supporting ongoing coaching. Lead dedicated group, building the team spirit, developing team style and behavior. Ensure resources for the studies assigned. Ensure that the workload of direct reports is adequate. Development and performance management of direct reports. Ensure that direct reports have development plans, according to IDP process. Coach the direct reports, and plans/organize coaching with external providers. Prepare salary and bonus proposals for direct reports based on their performance in close collaboration with responsible (Senior) Director, Country Head and local HRBP. Contribute to efficient SMM organization and its functioning at country level by working with responsible (Senior) Director, Country Head. Contribute to high-quality feasibility work. Oversee delivery of SMM study delivery country level targets to plan, with speed and quality. Contribute to the quality improvement of the study processes and other procedures. Ensure all systems are updated. Ensure completeness and timeliness of the eTMF to maintain it "Inspection Ready". Assist (Senior) Director, Country Head or Local Study ADs/ Local Study Teams in forecasting study timelines, resources, recruitment, study materials and drugs. Direct LSAD/ Local Study Teams on major study commitments including resolving any You Have: Bachelor's degree in related discipline in life science, or equivalent qualification. Minimum seven (7) years of experience in Development Operations (CRA / SrCRA / LSAD) or other related fields. Project management experience Excellent knowledge of spoken and written English. Adept to working with IT systems. Ability for national and international travel. Desired skills Knowledge of the Clinical Study Process,Monitoring Process and international ICH-GCP guidelines. Demonstrated experience with conflict management. Experience with the Study Drug Handling Process and the Data Management Process. Knowledge of relevant local and international regulations. Look for and promote more efficient methods/processes of delivering quality clinical trials with reduced budget and in less time. Background in Breast/Gyn therapeutic area. Work in an environment of remote collaborators. Good resource management and financial management skills. Benefits offered include: A qualified retirement program [401(k) plan] Paid vacation, holidays, and paid leaves Health benefits including medical, prescription drug, dental, and vision coverage following the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.The annual base salary for this position ranges from $162,000 to $243,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). #ClinicalOperations #LI-remote Date Posted 13-Feb-2026 Closing Date 16-Feb-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

ref: (R-241569) 18 days ago

Back to search results