serious business. But that doesn&#**Apply on the website**;t mean you
can&#**Apply on the website**;t have fun while you do it. With our
vision to be the partner of choice in drug development, we hire only
the best and brightest in the industry. Are you one of them?
As a Senior Project Manager Laboratory, you will ensure client
satisfaction by acting as the Client&#**Apply on the website**;s main
contact in all matters regarding ICON Central Laboratories services,
including the setup and day-to-day management of studies.
The role
Act as the sponsor&#**Apply on the website**;s main contact person in
all matters regarding our central laboratory services,following up and
responding to clinical study specific inquiries from Sponsors,
Physicians, CRA and CRO representatives and the ICON internal
departments.
Review newly assigned protocols and Amendments. Coordinate and manage
the completion of the Clinical Laboratory Worksheet (CLW) and
communicate information as required to other departments within ICON
Laboratories (and ICON Clinical CRO if appropriate).
Ensure that proper guidelines for communication are set at study
start-up and maintained throughout a study by creating and updating
the study Project Management PlanEnsure adherence to the protocol
specific monitoring plan. Maintain clinical study specific study files
and ensure that all appropriate documents are properly maintained.
Ensure that all necessary documents are archived at study closure.
Provide Sponsors with study management reports as required and agreed.
Provide client with support on ICOLabs and iSite systems.
Proactively monitor study budget through monitoring of Protocol
Tracking reports and other tools provided to assist
Regularly use the PM Dashboard to help monitor study progress and
communicate to Sponsors in a timely manner if issues identified may
require further investigation
Set the timelines for and monitor the progress of shipment requests
for storage samples and verify data.
Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off
Meeting, Bid Defenses or Face to Face Governance meetings.
Serve as a leader, mentor and consultant to more junior team members
in resolving issues orquestions as they arise.
Serve as a gateway for escalation of PM issues to PM Manager and
Senior/Executive Management
What you need
In depth proven experience working in a clinical laboratory, clinical
trials, or customer management/account management role in a life
sciences related organization
Prior relevant experience successfully performing a Project Management
role in a service area serving clinical trials, such as IVRS, Clinical
Supplies Packaging and Distribution, Medical Imaging, Data Management,
or Electronic Data Capture.
Successful management in providing technical services for multiple
clinical trials, including Presentation at Investigator Meetings,
Implementation of protocol amendments, Completion of Laboratory
Configurations, Trial reconciliations, Participation in
sponsor/regulatory audits, Bid Defenses
Bachelor&#**Apply on the website**;s degree or local equivalent in
Science, Business or related Field and/ or an alternative combination
of experience, education, and training.
Benefits of Working at ICONOther than working with an outstanding team
of ambitious people, we also offer a very competitive compensation
package. This varies from country to country so a dedicated recruiter
will discuss this with you at interview stage.
We care about our employees as they are the key to our success. We
provide an open and friendly work environment where we empower people
and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer and committed to providing a
workplace free of any discrimination or harassment.
EOE race/color/religion/sex/sexual orientation/gender
identity/disability/vet/national origin#LI-CW1 As a global provider of drug development solutions, our work is
serious business. But that doesn&#**Apply on the website**;t mean you
can&#**Apply on the website**;t have fun while you do it. With our
vision to be the partner of choice in drug development, we hire only
the best and brightest in the industry. Are you one of them?
As a Senior Project Manager Laboratory, you will ensure client
satisfaction by acting as the Client&#**Apply on the website**;s main
contact in all matters regarding ICON Central Laboratories services,
including the setup and day-to-day management of studies.
The role
Act as the sponsor&#**Apply on the website**;s main contact person in
all matters regarding our central laboratory services,following up and
responding to clinical study specific inquiries from Sponsors,
Physicians, CRA and CRO representatives and the ICON internal
departments.
Review newly assigned protocols and Amendments. Coordinate and manage
the completion of the Clinical Laboratory Worksheet (CLW) and
communicate information as required to other departments within ICON
Laboratories (and ICON Clinical CRO if appropriate).
Ensure that proper guidelines for communication are set at study
start-up and maintained throughout a study by creating and updating
the study Project Management PlanEnsure adherence to the protocol
specific monitoring plan. Maintain clinical study specific study files
and ensure that all appropriate documents are properly maintained.
Ensure that all necessary documents are archived at study closure.
Provide Sponsors with study management reports as required and agreed.
Provide client with support on ICOLabs and iSite systems.
Proactively monitor study budget through monitoring of Protocol
Tracking reports and other tools provided to assist
Regularly use the PM Dashboard to help monitor study progress and
communicate to Sponsors in a timely manner if issues identified may
require further investigation
Set the timelines for and monitor the progress of shipment requests
for storage samples and verify data.
Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off
Meeting, Bid Defenses or Face to Face Governance meetings.
Serve as a leader, mentor and consultant to more junior team members
in resolving issues orquestions as they arise.
Serve as a gateway for escalation of PM issues to PM Manager and
Senior/Executive Management
What you need
In depth proven experience working in a clinical laboratory, clinical
trials, or customer management/account management role in a life
sciences related organization
Prior relevant experience successfully performing a Project Management
role in a service area serving clinical trials, such as IVRS, Clinical
Supplies Packaging and Distribution, Medical Imaging, Data Management,
or Electronic Data Capture.
Successful management in providing technical services for multiple
clinical trials, including Presentation at Investigator Meetings,
Implementation of protocol amendments, Completion of Laboratory
Configurations, Trial reconciliations, Participation in
sponsor/regulatory audits, Bid Defenses
Bachelor&#**Apply on the website**;s degree or local equivalent in
Science, Business or related Field and/ or an alternative combination
of experience, education, and training.
Benefits of Working at ICONOther than working with an outstanding team
of ambitious people, we also offer a very competitive compensation
package. This varies from country to country so a dedicated recruiter
will discuss this with you at interview stage.
We care about our employees as they are the key to our success. We
provide an open and friendly work environment where we empower people
and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer and committed to providing a
workplace free of any discrimination or harassment.
EOE race/color/religion/sex/sexual orientation/gender
identity/disability/vet/national origin#LI-CW1
We need : English (Good)
Type: Permanent
Payment:
Category: Others
