Clinical Operations Manager

Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRA Manager opportunities. 

ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain. 

We are presently in over 40 countries with over 80 offices worldwide and over 11K employees globally. We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients. 

Overview of the Role 

We support our line CRA Managers to effectively manage our CRAs to ensure high performance, quality of monitoring and continue development. We offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, performance bonus and vacation. Additionally, we have cutting edge technology to ensure better outcomes. 

Our CRA Managers will ensure CRAs perform monitoring and site management responsibilities to an appropriate working standard including (but not limited to ): 
- updating study files 
- completing trip reports and follow-up letters in a timely manner 
- managing investigational product 
- completing source data verification 
- developing effective relationships with sites 

Monitor and evaluate CRA workloads and liaise with Resource Management, the relevant Project Manager and Director of Clinical Operations (as needed) to ensure appropriate allocation of resources and optimal utilization and workload.  Accompany CRAs to provide on-site training for pre-study, initiation, monitoring and close-out sites.  Conduct on-site Monitor Assessment Visits as required. Implement individual development and provide coaching and mentoring to assigned CRAs. 

Prior experience of managing CRAs. 
Fundamental knowledge of Clinical Research, and expertise in all phases of clinical trail. 
Comprehensive knowledge and understanding of ICH-GCP. 
Previous experience in delivering training. 
Ability to liaise successfully with clinical project teams and other relevant departments. 

Requirements 
Bachelors’ Degree or local equivalent in, life sciences, medicine or related discipline 
Minimum of six ( 6) years of clinical research experience with at least four 
(4) years of relevant experience as a Senior CRA or Principal CRA (in a Lead CRA role) or at 
least two ( 2) years as a Project Manager CRA Manager or equivalent job role. 

We invite you to review our clinical opportunities at www.iconplc.com/careers.

We provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability.