Nonclinical Project Manager
We are the leading oncology CRO, developing novel treatments for patients that need them most. Our team is fully dedicated to oncology – it is all we do – combining innovation and expertise to quickly move medicines from preclinical development into clinical trials. Adaptive and forward-thinking – we guide our client's therapy through the most critical development milestones from the lab to planning their regulatory and clinical strategy. Our ultimate goal? To help patients.
Position Summary:
The TD2 nonclinical project manager primarily functions as a liaison between TD2 scientific staff and external clients. The project manager collaborates with laboratory staff and data specialists to ensure adherence to timelines, milestones, and protocols as well as delivery of high quality data to clients. The project manager works closely with clients to gather information for protocol development, ensure successful study execution, troubleshoot technical aspects of project, and provide project updates routinely.
Essential Functions:
Communicates details of nonclinical studies to clients
Involved in pre-study preparation
Manages nonclinical study timelines, milestones, and overall status throughout project
Troubleshoots and discusses execution and technical aspects of project in conjunction with TD2 technical staff.
Compiles weekly data updates in conjunction with data specialists and provides to clients
Quality control of collected data and study reports
Summarizes study data in study reports in conjunction with data specialists
Critical assessment of data to ensure data accuracy
Works with clients to gather data, develop study protocol, and create study budgets
Maintains positive rapport with clients
Actively participates in meetings and on calls with clients
Cultivates sponsor relationship to encourage repeat business
Tracks internal business metrics
Performs other duties as assigned
Job Requirements:
Bachelor’s degree in a science-related field and 3-5 years direct work experience in biotech or pharmaceutical industry
Technical laboratory experience in nonclinical drug development preferred
Experience with nonclinical oncology project management preferred
Strong computer skills, including proficiency in the use of Microsoft applications
Strong attention to detail
Highly organized
Excellent communication skills and ability to work with a variety of personalities successfully
Ability to work independently in a fast-paced environment.
Able to set priorities and meet deadlines.
TD2 is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, creed, disability, veteran’s status, gender, sexual orientation, gender identity, or gender expression.
About the job
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Nonclinical Project Manager
We are the leading oncology CRO, developing novel treatments for patients that need them most. Our team is fully dedicated to oncology – it is all we do – combining innovation and expertise to quickly move medicines from preclinical development into clinical trials. Adaptive and forward-thinking – we guide our client's therapy through the most critical development milestones from the lab to planning their regulatory and clinical strategy. Our ultimate goal? To help patients.
Position Summary:
The TD2 nonclinical project manager primarily functions as a liaison between TD2 scientific staff and external clients. The project manager collaborates with laboratory staff and data specialists to ensure adherence to timelines, milestones, and protocols as well as delivery of high quality data to clients. The project manager works closely with clients to gather information for protocol development, ensure successful study execution, troubleshoot technical aspects of project, and provide project updates routinely.
Essential Functions:
Communicates details of nonclinical studies to clients
Involved in pre-study preparation
Manages nonclinical study timelines, milestones, and overall status throughout project
Troubleshoots and discusses execution and technical aspects of project in conjunction with TD2 technical staff.
Compiles weekly data updates in conjunction with data specialists and provides to clients
Quality control of collected data and study reports
Summarizes study data in study reports in conjunction with data specialists
Critical assessment of data to ensure data accuracy
Works with clients to gather data, develop study protocol, and create study budgets
Maintains positive rapport with clients
Actively participates in meetings and on calls with clients
Cultivates sponsor relationship to encourage repeat business
Tracks internal business metrics
Performs other duties as assigned
Job Requirements:
Bachelor’s degree in a science-related field and 3-5 years direct work experience in biotech or pharmaceutical industry
Technical laboratory experience in nonclinical drug development preferred
Experience with nonclinical oncology project management preferred
Strong computer skills, including proficiency in the use of Microsoft applications
Strong attention to detail
Highly organized
Excellent communication skills and ability to work with a variety of personalities successfully
Ability to work independently in a fast-paced environment.
Able to set priorities and meet deadlines.
TD2 is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, creed, disability, veteran’s status, gender, sexual orientation, gender identity, or gender expression.