Best Practices, Biology, Biotech and Pharmaceutical, Clinical Laboratory, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Continuous Improvement, Contract Management, Contract Research Organization (CRO), Cross-Functional, Customer Relations, Documentation, Editing, Laboratory Testing, Meeting Minutes, Organizational Skills, Plan Meetings, Process Flow, Project Development, Project Planning, Project Tracking, Project/Program Management, Team Player, Test Lab, Time Management
Type: Contract, W2 only
Duration: 12+ months
Location: remote
Pay: $35/hr-$37/hr
Please note that at this time we are unable to sponsor employment authorization (both new and transfer)
Clinical Science Program Specialists in CDx Pharma Services.
Responsibilities:
- Manage multiple clinical testing and lab services projects from initiation through contract completion under supervision of Program Manager. Act as primary point of contact to Pharma customers.
- Perform tactical coordination of timelines for all projects and functions within CDx Pharma Services.
- Develop project plans, establish and coordinate timelines for assigned projects and functions.
- Manage execution of cross-functional plans and tracks progress of activities.
- Identify gaps, potential bottlenecks or delays and challenge assumptions.
- Oversee and guide day to day activities of sample process flow and accurate reporting of results.
- Implement / pull in best practices within the clinical sciences team; foster continuous improvement by ensuring knowledge and experience exchange.
- Guide and manage cross-functional interactions to complete the assigned projects within the deadline.
- Interface with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serve as single point of contact with Pharma and company clients.
- Manage meeting activities such as setting agendas, organizing meeting time and editing meeting minutes.
Qualifications:
- At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation.
- Exposure to clinical studies.
- Experience with clinical projects that require rapid activity/milestone achievement.
- Strong communication, collaboration, and organizational skills are required
- Bachelor's degree is required (Life Sciences is preferred).
Preferred:
- Previous experience with standard project management process.
- Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow.
- Experience in clinical studies or companion diagnostics.
- Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge.
We are an Equal Opportunity employer and welcome talent across all aspects of background, orientation, origin, and identity in an inclusive and non-discriminatory way. Applicants receive consideration without bias and based on the relevant qualifications, talents, skills, experiences, and business needs.