Contract Clinical Trial Manager
Company Name:
BioBridges, LLC
Overview
Our client is a biopharmaceutical company at the forefront of therapies for rare and orphan diseases.
Their Clinical Divide
The Clinical Project Manager will lead, plan, manage, and ensure successful completion of routine to complex clinical studies.
Project Details
Responsibilities include:
Primary point of contact for studies.
Participate in Protocol Writing and CRF Design
Manage all vendors, on spec, on time, on budget (including leading calls and review of invoices)
Oversee site selection
Develop and manage study timelines and budgets utilizing MS Project
Calculate drug supply needs, liaise with Tech Ops
Plan Investigator Meetings
Gather site information from Site Manager to have an understanding of each site in the study
Create strategy for patient recruitment and retention
Maintain and report metrics
Develop direct reports
Liaise with QA on Quality (including CAPAs and Metrics)
Requirements:
Minimum of Bachelors Degree, Nursing Degree preferred.
Professional Work Experience
o 4
years experience from similar work within a pharmaceutical company or CRO is preferable, but can also have experience as a research coordinator (desired)
o Previous monitoring experience
o Travel 50%
Scope
Contract duration 9 months. Will be required to work onsite in their office when not travelingEstimated Salary: $20 to $28 per hour based on qualifications.
BioBridges, LLC
Overview
Our client is a biopharmaceutical company at the forefront of therapies for rare and orphan diseases.
Their Clinical Divide
The Clinical Project Manager will lead, plan, manage, and ensure successful completion of routine to complex clinical studies.
Project Details
Responsibilities include:
Primary point of contact for studies.
Participate in Protocol Writing and CRF Design
Manage all vendors, on spec, on time, on budget (including leading calls and review of invoices)
Oversee site selection
Develop and manage study timelines and budgets utilizing MS Project
Calculate drug supply needs, liaise with Tech Ops
Plan Investigator Meetings
Gather site information from Site Manager to have an understanding of each site in the study
Create strategy for patient recruitment and retention
Maintain and report metrics
Develop direct reports
Liaise with QA on Quality (including CAPAs and Metrics)
Requirements:
Minimum of Bachelors Degree, Nursing Degree preferred.
Professional Work Experience
o 4
years experience from similar work within a pharmaceutical company or CRO is preferable, but can also have experience as a research coordinator (desired)
o Previous monitoring experience
o Travel 50%
Scope
Contract duration 9 months. Will be required to work onsite in their office when not travelingEstimated Salary: $20 to $28 per hour based on qualifications.
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