Location: 1910 East Innovation Park Dr, Tucson, AZ 85755
Shift: Fully Remote - Monday – Friday, 8 Hours/Day
Contract Length: 12 Months (Extension or Conversion Possible)

This is an exciting opportunity to join Our Client, a global leader in biotechnology and pharmaceutical research, development and patient care initiatives that help millions of people every day. If you are interested in starting a career with one of the world's largest and most innovative biotech companies- this is the job for you!

Job Description

• 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 and: develop project plans establish and coordinate timelines for assigned projects and functions, manage execution of cross-functional plans and track progress of activities, and 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 clinical sciences team and foster continuous improvement by ensuring knowledge and experience exchange
• Guide and manage cross-functional interactions to complete assigned projects within the deadline
• Interface with resources outside the company and serve as a single point of contact with clients
• Manage meeting activities such as setting agendas, organizing meeting times, and editing meeting minutes
• Track, maintain, and communicate project reports and clinical study data to clients
• Other duties as assigned by management

Skills and Experience:

• Experience with clinical trials that require rapid activity/milestone achievement
• Experience in clinical trial management and knowledge of bio-sample management and process flow preferred
• Experience with standard project management process desired
• Diagnostic and/or pharmaceutical industry and relevant diagnostic area knowledge preferred
• Clinical trial coordination/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
• Some travel may be required based on business needs

Education:

• Bachelor’s degree in a related field or 2 years of work experience in a related field
• Master’s Degree with specific Project Management Training, or Clinical Research Training and/or certification

Our Client also requires that all individuals placed on assignment in this role to be fully vaccinated against COVID-19 or have a legal exemption or an accommodation in compliance with the Americans with Disabilities Act. An individual is considered fully vaccinated against COVID-19 two weeks after either of the following: Receipt of the second dose of the two-shot series vaccine from Moderna or Pharmaceutical; or receipt of the single dose vaccine from Pharmaceutical.

#RLI

Job Type: Contract

Pay: $34.00 - $37.46 per hour

Benefits:

• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Work Location: Remote

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