SeniorScientific Project Manager

The Sr. / Scientific Project Manager will be responsible for providing project management oversight to a biopharmaceutical client tasked with managing and executing analytical testing method development and/or validation of such assays as immunoassays bioassays pharmacokinetic and/or flow cytometry assays under Good Laboratory Practices (GLP). He/she will provide project management and technical support to teams conducting training technical transfer data review and trending analysis. The Sr. Project Manager must have the ability to effectively monitor the performance of CROs and service providers. The incumbent will also be responsible for operational documentation including SOPs validation protocols and reports transfer protocols and reports and management reports.

What will you do

• Vendor Management:
  • Lead the contracting with thirdparty lab service providers for assay development and validation.
  • Collaborate with business operations procurement and clinical teams to ensure appropriate SOWs and contracts.
• Study Coordination:
  • Manage critical reagent supply and sample analysis.
  • Work closely with bioanalytical strategy leads clinical trial teams and lab service providers to finalize study documents and meet timelines.
  • Support the development of novel Bioanalytical processes.
• Documentation and Data:
  • Provide input into clinical trial documents (e.g. eCRFs ICFs SOWs).
  • Drive the delivery of data transfer specifications and ensure data accuracy.
• Sample Logistics:
  • Track and reconcile sample testing resolving any issues that arise.
  • Contribute to cleaning and finalizing data.

What will you bring to the table

• Bachelors or Masters level equivalent degree in Life Sciences or related field required
• 2 3 years experience in the drug development and/or clinical trial processes for Scientific Project Manager required
• 5 6 years experience in the drug development and/or clinical trial processes for Senior Scientific Project Manager required
• Equivalent amount of experience managing projects including timelines budgeting and forecasting
• Experience with method development validation and troubleshooting
• Extensive knowledge and experience in bioanalysis within regulatory environments (GLP/ GCP) to include experience with PK/ADA and/or biomarker analysis
• Experience working in Oncology is preferred
• PMP certified and formal change management training strongly preferred
• Highly proficient in MS Office Suite including MS Project Word Excel and PowerPoint Smartsheet and SharePoint
• Strong planning attention to detail communication and organizational skills
• Excellent verbal and written communication skills

Working Hours Location Travel:

• Ability to be onsite in Cambridge UK Monday Friday for the first few weeks of orientation
• Upon completion of orientation position will be remote with the ability to come into the office as needed for meetings
• Candidates must be within a commutable proximity toCambridge UK.

Read more below and get ready for your next great employment adventure!

Some of the Perks our LabConnectors Love:

• We truly live our values:partnership excellence collaboration forward thinking accountability informed andnimble
• The ability to make an impact on a passionate and growing team
• Great communication on a smaller sized team
• A market based salary
• Tools to effectively do your job (laptop phone reimbursement)

We are a growing and global team on a mission to create healthier communities by accelerating the development of new medicines. In addition to great perks and challenging work assignments we invest in our people with enriching career growth opportunities.

We believe in a friendly and collaborative environment with open lines of communication. Join our team and discover how your work can impact the lives of people all over the world.

It is the policy of LabConnect to provide equal employment opportunities without regard to race color religion sex sexual orientation gender identity national origin age disability marital status veteran status sexual orientation genetic information or any other protected characteristic under applicable law.

Equal Employment Opportunity Posters:


If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application please emailor call.

For more information visit