Clinical Science Program Specialist

Job Description

Job Description

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.