Acerta Pharma is a leader in the field of covalent binding technology and is applying this technology to create novel, highly selective therapies for cancer. In February 2016, AstraZeneca acquired a majority share of Acerta Pharma via a USD $4 billion investment and is a committed partner to the development of these innovative drug candidates.
Acalabrutinib is Acerta's lead program which was developed based on our discovery efforts. It is an investigational covalent Bruton tyrosine kinase (BTK) inhibitor currently under investigation in multiple Phase 3 clinical trials. The clinical program includes over 20 trials in hematologic malignancies and solid tumors. Over 1,800 patients have participated in these trials to date.
The Associate Director, Clinical Operations role encompasses a key role in setting and executing on departmental strategy, as well as managing the day-to-day functioning of assigned teams within the Clinical Operations Department.
The Associate Director, Clinical Operations is responsible for program related work and represents Clinical Operations at the Global Development team and Global Product teams as required. Ensuring protocols can be executed in a compliant manner by Clinical Operations through optimization of assessments, oversight of clinical operations aspects of a clinical protocol . Performs and assists in Sponsor pre-site, site and audit assessments. Provides budget, timeline and feasibility support for study protocols until a study team can be established. Interfaces with key departments to discuss status of current studies, as well as significant staffing, hospital and recruitment issues. Explores potential upcoming studies, methods for continuing to provide sponsors with the highest quality data, increasing clinic efficiency and setting directions for future growth. Oversees clinical trials and study teams to ensure protocols are executed on time, to budget and with quality. Establishes and maintains relationships with service providers. Negotiates contracts/ rates with identified service providers. Works closely with study team on recruitment strategy/issues.
Additionally, the Associate Director, Clinical Operations role entails department related work developing, implemting, monitoring, and supporting Standard Operating Procedures (SOPs) and work processes to ensure an efficient Clinical Operations department. Maintains oversight for Clinical Operations staff to establish clear expectations for staff performance, clear delineation of accountability for tasks and processes, and consistent monitoring of work product. Meets regularly with Clinical Operations Management to discuss staffing for upcoming studies, sharing of staff between departments, and performance of staff. Oversees all hiring, transfers, performance reviews, increases, and terminations in the department for in/direct reports. Organizes and/or participates in clinical operations department meetings. Reviews, tracks and approves all departmental expenses for in/direct reports. Maintains and participates in the fiscal objectives of Clinical Operations and recognizes cost reduction opportunities. Manages all aspects of departmental performance improvement strategies including: identifying areas for improvement, developing an action plan in conjunction with all affected areas/staff, and tracking and reporting results to Senior Management. Oversees and approves the review, revision, and/or retirement of departmental objectives. Maintains and updates knowledge of Good Clinical Practices (GCPs) and their proper application. Reinforces the use of GCPs departmentally through example and staff training. Provides support to Business Development and other functions as appropriate. Represents Clinical Operations and company at conferences and meetings as appropriate.
* Bachelor or Master's Degree in a health-related field
* Eight (8) years related experience in life sciences, including clinical development experience.
* Proven track record as a leader in clinical trials in the biotech or pharmaceutical industry.
* Experience and knowledge of ICH-GCP and other relevant regulations
* Computer proficiency
* Demonstrated leadership ability
* Meticulous attention to detail
* Strong interpersonal, written/ verbal communication and organizational skills
* Ability to effectively manage time, resources and multi-task
Next Steps -- Apply today!
To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience -- it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.
A little about us:
MedImmune is the global biologics research and development arm of AstraZeneca