Csr Clinical Study Administrator

Clinical Study Administrator, Country Operations Management This is what you will do: The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements. 
The CSA collaborates closely with the Project Manager Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country.
You will be responsible for: Providing support to the local study team in COM in achieving quality and timeliness of study deliverables across the lifecycle of assigned trials (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the Clinical Trial Management System (CTMS) and other general trial support in the country or region as delegated or per assigned trials. Providing support to the local study team including for start up activitiesin start-up phase: CDA delivery and negotiation, distribution and collection of documents, communication with sites during contract negotiation phase, Site File preparation, and preparation and approval of sites for activation, etc Collaborating with PMCO, CRAs, SSU managerand study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information Act as a central point of contact for the local study teamin COM for designated project communications, correspondence, and associated documentation. Input on the development and maintenance of project management and other global tracking tools (e.g: CTMS, smartsheets, etc). Collaborating in global initiatives to standardize processes within and across countries (collaboration with other local and global CSAs) Assist with local language translations, IRB/CEC/CA submissions in collaboration with Regulatory Affairs and other functions, as required within the country/region. Providing support to local COM team with local Face-to-Face study and team meetings (venue, cost, agenda, etc), support team teleconferences, assist with staff onboarding as required by country/region Depending on the country/region, the CSA may provide varying levels of COM support to the department rather than to assigned studies as needed. You will need to have: Bachelor's Degree in a related discipline, preferably life science. Proficiency with MS Office Suite (excel, word, powerpoint) Understanding of the drug development process either via education or experience in the life sciences field. Preferably minimum experience of 1 year in Development Excellent collaboration and interpersonal skills, unafraid to ask questions. Strong organizational skills and ability to manage competing priorities. Strong attention to detail Effective written and verbal communication skills We would prefer for you to have: Prior experience working in clinical research Medical knowledge and ability to learn relevant Alexion rare disease areas. Ability to work in an environment of remote collaboratorsand in amatrix reporting structure Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business. Ability to look for and champion more efficient and effective methods/ processes of delivering quality clinical trials with reduced budget and in less time. Team oriented and flexible; ability to respond quicky to shifting demands and opportunities Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment. This is what you will do: The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements. 
The CSA collaborates closely with the Project Manager Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country.
You will be responsible for: Providing support to the local study team in COM in achieving quality and timeliness of study deliverables across the lifecycle of assigned trials (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the Clinical Trial Management System (CTMS) and other general trial support in the country or region as delegated or per assigned trials. Providing support to the local study team including for start up activitiesin start-up phase: CDA delivery and negotiation, distribution and collection of documents, communication with sites during contract negotiation phase, Site File preparation, and preparation and approval of sites for activation, etc Collaborating with PMCO, CRAs, SSU managerand study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information Act as a central point of contact for the local study teamin COM for designated project communications, correspondence, and associated documentation. Input on the development and maintenance of project management and other global tracking tools (e.g: CTMS, smartsheets, etc). Collaborating in global initiatives to standardize processes within and across countries (collaboration with other local and global CSAs) Assist with local language translations, IRB/CEC/CA submissions in collaboration with Regulatory Affairs and other functions, as required within the country/region. Providing support to local COM team with local Face-to-Face study and team meetings (venue, cost, agenda, etc), support team teleconferences, assist with staff onboarding as required by country/region Depending on the country/region, the CSA may provide varying levels of COM support to the department rather than to assigned studies as needed. You will need to have: Bachelor's Degree in a related discipline, preferably life science. Proficiency with MS Office Suite (excel, word, powerpoint) Understanding of the drug development process either via education or experience in the life sciences field. Preferably minimum experience of 1 year in Development Excellent collaboration and interpersonal skills, unafraid to ask questions. Strong organizational skills and ability to manage competing priorities. Strong attention to detail Effective written and verbal communication skills We would prefer for you to have: Prior experience working in clinical research Medical knowledge and ability to learn relevant Alexion rare disease areas. Ability to work in an environment of remote collaboratorsand in amatrix reporting structure Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business. Ability to look for and champion more efficient and effective methods/ processes of delivering quality clinical trials with reduced budget and in less time. Team oriented and flexible; ability to respond quicky to shifting demands and opportunities Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment. Date Posted
20-Nov.-2024 Closing Date
24-Nov.-2024 Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact . Alexion participates in E-Verify.