Director – IT Support
New position that will lead an applications support to group within the Pharmaceutical industry. This person will have experience leading the RFP process and setting up SLAs with vendors for managed services. Must have experience managing direct reports.
IT Business Analyst – CRM
IT Business analyst to sit between a pharmaceutical salesforce and the IT team. This person will have experience with UAT and working closely with the business.
Technical Analyst – CRM
Technical Analyst working in either Veeva or Salesforce.com. Very technical role with business interaction.
Sr Director of Commercial Transparency and Speaker Programs
Must have experience leading both the sunshine act compliance as well as Speaker Bureau.
IT Business Relationship Manager
New position looking for someone that can work with the business on their needs and then bring the agreed upon needs to IT. Act in a intermediary / Account Management capacity.
Director – Marketing Technology
Able to set up and run a new Pharmaceutical Digital technology program. Must have both the business and IT experience to lead the group.
Clinical Trial Manager
Functions as the clinical study team leader to plan, organize, and coordinate all operational aspects of a clinical study from protocol development through database lock. Ensures timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials.
This individual is responsible for performing domestic and international audits/inspections that ensure compliance with the FDA and other worldwide health authority regulations/guidelines, site SOPs, protocols, and industry standards, as applicable. The Director – GCP acts as a compliance resource to associates and provides recommendations for corrective action and tracks corrective action commitments until closure.
IT Compliance Analyst
IT Compliance Analyst is responsible for ensuring that the IOPS IT group is operating in compliance with regulatory requirements and internal procedures as well being the key liaison between the IOPS IT and Quality Assurance groups.
Works with end users to develop Electronic Notebook (ELN) project requirements. Configures the ELN to meet end-user needs. Processes system change control, documents configuration, and writes test plans. Provide end-user support for ELN including troubleshooting and user training.
Sr. Manager, Commercial Systems
Responsible for the management of the Customer Master, the integrity of the data housed therein and the associated data exchanges both with internal systems and with vendor-partners. The person in this role is also is responsible for ensuring that the CRM (“customer relationship management system”) fully meet the needs of the business, primarily its use by the Field-based teams, and that associated policies and processes are effectively implemented and maintained.
Director – GLP Quality Assurance and Validation
Manages and coordinates GLP regulated QA activities and validation activities for computer systems and equipment used for GLP and GMP regulated projects. This individual is responsible for independently performing domestic and international audits/inspections that ensure compliance with the FDA and other worldwide health authority regulations/guidelines, site SOPs, protocols, and industry standards, as applicable.
Oncology focused PhD or Pharm.D for a biotech company looking to get their Regulatory function established. This person will also interact with the FDA.
Sr. Director of Safety
Oncology focused MD who has built a safety function within another organization. This person needs to be both operational and strategic.
Senior Director of Procurement
Responsible for building their Global procurement and sourcing function. This person will have experience building their strategic sourcing activities (form, facilitate and lead procurement teams) focusing on Asia. This person will have the experience and capability to create analytics and dashboards around their sourcing activities. You will need to set up systems, build a team, have experience with direct and indirect spend along with global experience.