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Scientific Project Coordinator

Project ManagerProject ManagerFull TimeRemoteMid LevelTeam 501-1,000

Location

United States

Posted

29 days ago

Salary

0

Seniority

Mid Level

No structured requirement data.

Job Description

Scientific Project Coordinator

LabConnect

Role Description LabConnect has an immediate opening within FSP Solutions for a Scientific Project Coordinator. This person will be responsible for providing operational oversight and support for outsourced analytical testing in ADA and PK bioanalysis. Support will include: - Monitoring timelines - Managing documentation and contracts - Maintaining tracking logs - Working with external vendor partners - Facilitating communications - Participating in all aspects of a study life cycle from initiation to closure Responsibilities - Manage analytical method support documentation including dosing documents, reagent qualifications, reagent expiry extensions, and bioanalytical reports. - Manage study timelines and monitor scheduling and conduct of bioanalytical testing to ensure alignment with data transfer deliverable requirements. - Assist with monitoring outsourced bioanalytical method performance and identifying analytical trends. - Communicate project updates and issues to cross functional teams including scientific project managers, internal scientists, CRO staff and operational teams. - Manage and lead recurring cross-functional meeting series. - Assist in facilitating contracts with external suppliers. - Support shipping and reagent requests. - Maintain trackers related to issues and program-specific information. - Support sample disposition requests. - Contribute to the maintenance of external collaboration sites. - Manage logistics for new clinical study initiation. - Participate in and/or lead operational process improvements. Qualifications - B.S., Life Sciences or related field. Master's Degree and/or 2 year degrees may be considered with different levels of work experience. - 4 years of industry-relevant project and/or laboratory management experience, required. - 1 - 3 years of Large Molecule PK/ADA/NAb Bioanalytical bench experience preferred (validation experience in the laboratory is a plus). - Demonstrated project and timeline management skills. - Proactive mindset/self-starter. - Solid organizational skills with attention to detail and ability to develop and follow process. - Strong oral and written communication skills with experience in both strong team collaboration and technical writing. - Experience working with vendors/service providers. - Understanding of clinical trial processes. - Working knowledge of Good Laboratory Practices (GLP), Good Clinical Practices (GCP) and/or Clinical Laboratory Improvement Amendments (CLIA). - Strong computer literacy, including word processing, SharePoint, presentation, and spreadsheet applications. - Ability to work effectively in a cross-functional team matrix environment. Work Hours/Travel - 100% remote with the ability to travel to the client site up to approximately 1 - 2 times per year, on the west coast. - Occasional meetings later in the day may be necessary to accommodate west coast hours. Benefits - Financial Security (Base Pay, 401k Match and Possible Annual Bonus Eligibility). - Health Benefits beginning on date of hire. - PTO plan, plus 11 Paid Company Holidays, and 1 Day to Volunteer in your community. - Short and Long-Term Disability, Life Insurance, and AD&D.

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