Jobs at Delta-Pharma

Job Title: TMF Manager Position Description This position is responsible for management of Clinical and other sections of the Trail Master Files (TMF), utilizing records management best practices and appropriate technologies. The individual will provide leadership and expertise in records management and archiving support for clinical research work. Including the completeness, safekeeping and acces...
full job description

Job Title: Clinical Data Manager Position Description The Clinical Data Manager (CDM) is responsible for the creation, updating, maintenance and validation of clinical study databases and for the provision of computerized reports of these data. The CDM is a key member of the clinical project team and will prioritize work in line with departmental and organizational management decisions. The respon...
full job description

Job Title: Recruiting Coordinator Position Description The Recruiting Coordinator is responsible for the administration of employment process in accordance with hiring guidelines and policies. The Coordinator provides support to the TA recruiting tam in various, customer-serving aspects of employment. The role requires extensive interaction with Hiring Managers, TA and candidates/applicants. This ...
full job description

Job Title: Clinical Trial Associate Position Description Supports project clinical teams by performing tasks related to study mgt from start up to study completion. Distributes, collects and tracks study documentation and completes project deliverables accurately and within project timelines. Key role in supporting project team needs. Utilizes technology effectively to support clinical development...
full job description

Job Title: SRA II, Analytical Chemistry Position Description With reasonable supervision, support drug discovery programs by providing instrument maintenance and troubleshooting support and in-depth qualitative / quantitative analysis of test compounds Position Responsibilities Serve as first responder to chemist request for instrument support, troubleshooting and problem Perform basic instrument ...
full job description

Job Title: Global Clinical Study Manager Position Description Oversee Phase IV and PMS studies to support multiple brands in CV-Met, Immuno, Virology and Neuroscience. Position Responsibilities Demonstrates a strong operational understanding of conducting clinical trials. In conjunction with Medical Strategy and Field Medical Science (FMS) executes or oversees outsourced Phase IV and Post Marketin...
full job description

Job Title: Product Safety Expert Position Description Accurate & timely reporting, effective investigations, proper analysis, timely filing of Adverse Events and compliance with international (e.g. FDA, ISO), regional (e.g. MDD) & country (e.g.France,Japan) regulations. Position Responsibilities Apply technical knowledge to provide direction and coordinate additional complaint activities with inte...
full job description

Job Title: Clinical Research Associate Position Description: As primary liaison between Company and the investigator, performs on-site monitoring visits and associated planning and follow-up activities; works with the Manager, Clinical Operations, Clinical Research Manager and other members of the clinical project team in the planning and execution of clinical trials Position Responsibilities Part...
full job description

Job Title: CRA - B Position Description The Clinical Research Associate (CRA) designs, implements, and monitors clinical studies of new and modified Company and competitive products. Ensures that the clinical studies of Company products are designed to validate product performance claims and support the products intended use. Prepares clinical data reviews and data summaries. Participates in the p...
full job description

Job Title: Regulatory Affairs Manager Position Description An individual in this role is expected to coordinate all aspects of CMC regulatory submissions relevant to their assigned projects. An individual in this role will serve as the regulatory CMC representative on matrix teams, as appropriate. Position Responsibilities Monitor changes to development plans and work with supervisor to design glo...
full job description

Job Title: Senior Biostatistician Position Description The Senior Statistician partners with Senior Statistical Scientists to contribute to clinical development projects, including study design and implementation topics, data analyses and CSR preparation. Position Responsibilities Study Planning: Reviews study protocols, authors statistical sections of protocols, prepares the study randomization, ...
full job description

Job Title: Clinical Data Manager Position Description The Clinical Data Manager (CDM) is responsible for the creation, updating, maintenance and validation of clinical study databases and for the provision of computerized reports of these data. The CDM is a key member of the clinical project team and will prioritize work in line with departmental and organizational management decisions. The respon...
full job description

Job Title: Quality Project Manager Position Description Manage and support knowledge management, metrics reporting, and continuous improvement projects in the areas of quality and compliance. Position Responsibilities Improve and maintain the Quality Operations Community intranet site (SharePoint) Research current industry issues (e.g., Warning Letters, FDA organizational changes, new regulations)...
full job description

Job Title: Regulatory Affairs Manager Position Description Serves as a liaison between the company and regulatory agencies for all assigned projects and is responsible for day to day regulatory support. Expected to provide guidance within Regulatory Affairs and to data generating departments to ensure timely filing and approval/maintenance of assigned programs. Position Responsibilities Responsibl...
full job description

Job Title: Associate/ Sr. Associate Regulatory CMC Position Description This position is responsible for supporting regulatory CMC submissions worldwide for commercial biologic products. Position Responsibilities Work with partners to determine submission requirements in each region. Coordinate the preparation and submission of international (ROW) regulatory CMC submissions. Coordinate response to...
full job description

Job Title:Medical Information Specialist Position Description The position is responsible for managing and providing product medical information used by external customers in the healthcare industry. Position Responsibilities Responsible for researching and responding to unsolicited request for medical information pertaining to the companies marketed and late stage investigational product Abstract...
full job description