Medical Alliances Operations Leader / ro-446

Location
CH-Basel
Start
asap (latest 01.10.22)
End
12 months
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
1900

Deadline:

Deadline
05.08.22; 9am.

 

Medical Alliances Operations Leader / ro-446

Location
CH-Basel
Workload
100 %

Start

asap (latest 01.10.22)

End

12 months

DEADLINE

Deadline
05.08.22; 9am.

  • CH-Basel
  • CH-Baseasap (latest 01.10.22)12 months100 % 1900rate negotiableDeadline
    05.08.22; 9am.

For our customer located in Basel/Switzerland we are currently looking for a: Medical Alliances Operations Leader (m/f/x)

 

Background:

 

MAOL is the PDMA Medical Alliances Operations role responsible for providing the operational expertise and leadership to one or more cross-functional investigator initiated study (IIS) / institution sponsored research (ISR) / Real-World-Data (RWD) studies management / responsible teams to ensure the effective and efficient delivery of all operational aspects of one or more studies through all phases of Clinical Study Management (Start-up, Conduct, Close), in accordance with the appropriate quality standards including ICH/GCP, GVP, applicable regulations and contract with Alliance Partners. The MAOL takes the initiative, launch new projects, and lead activities within PDMA Medical Alliances Operations and the IIS / ISR / RWD Community of Practices and Chapters

 

Ideal candidate:
We are looking for a MAOL to replace a team member leaving. This person will be supervising and overseeing studies in partnership with academic sponsors. The successful candidate will have at least a Bachelor in life sciences (or business administration with relevant experience, we are looking for someone with minimum 3 to 5 years of relevant experience in international clinical project management, across all phases and within Oncology. This person should be experienced in evidence generation.

 

General Information:

  • Start date: ASAP
  • Latest possible start date: 2 months’ notice period
  • End date: 12 months duration
  • Extension: possible
  • Workplace: Basel
  • Workload: 100%
  • Onsite/Home Office: Flexible
  • Travel: +/- 10%
  • Department: PDMA Medical Alliances Operations (MAO) (MDAF)

Tasks & Responsibilities

  • Provides direction and leadership to one or more study management / responsible teams or squads
  • Responsible and/or contributes to the development and management of the study timelines, resources, budget, risk and quality plans
  • Provides clinical operations expertise to ensure operational feasibility and delivery
  • Oversees forecasting of clinical/non-clinical supplies
  • Delivers the operational elements of the study plan
  • Identifies areas of best practice and process improvements
  • Ensures study adherence to ICH/GCP, GVP, internal policies and SOPs Compliance
    Please make sure to read the attached full job description.

Must Haves

  • Minimum 3 to 5 years of relevant experience in international clinical project management
  • Experience working with studies in all phases and experience in evidence generation 
  • Oncology experience
  • Education: minimum Bachelor level ideally in Natural/Life Sciences (please note Business Administration plus relevant experience is considered)

Nice to Haves

  • Experience in Breast Cancer and/or Gynecology

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Basel
  • CH-Baseasap (latest 01.10.22)12 months100 % 1900rate negotiableDeadline
    05.08.22; 9am.

For our customer located in Basel/Switzerland we are currently looking for a: Medical Alliances Operations Leader (m/f/x)

 

Background:

 

MAOL is the PDMA Medical Alliances Operations role responsible for providing the operational expertise and leadership to one or more cross-functional investigator initiated study (IIS) / institution sponsored research (ISR) / Real-World-Data (RWD) studies management / responsible teams to ensure the effective and efficient delivery of all operational aspects of one or more studies through all phases of Clinical Study Management (Start-up, Conduct, Close), in accordance with the appropriate quality standards including ICH/GCP, GVP, applicable regulations and contract with Alliance Partners. The MAOL takes the initiative, launch new projects, and lead activities within PDMA Medical Alliances Operations and the IIS / ISR / RWD Community of Practices and Chapters

 

Ideal candidate:
We are looking for a MAOL to replace a team member leaving. This person will be supervising and overseeing studies in partnership with academic sponsors. The successful candidate will have at least a Bachelor in life sciences (or business administration with relevant experience, we are looking for someone with minimum 3 to 5 years of relevant experience in international clinical project management, across all phases and within Oncology. This person should be experienced in evidence generation.

 

General Information:

  • Start date: ASAP
  • Latest possible start date: 2 months’ notice period
  • End date: 12 months duration
  • Extension: possible
  • Workplace: Basel
  • Workload: 100%
  • Onsite/Home Office: Flexible
  • Travel: +/- 10%
  • Department: PDMA Medical Alliances Operations (MAO) (MDAF)

Tasks & Responsibilities

  • Provides direction and leadership to one or more study management / responsible teams or squads
  • Responsible and/or contributes to the development and management of the study timelines, resources, budget, risk and quality plans
  • Provides clinical operations expertise to ensure operational feasibility and delivery
  • Oversees forecasting of clinical/non-clinical supplies
  • Delivers the operational elements of the study plan
  • Identifies areas of best practice and process improvements
  • Ensures study adherence to ICH/GCP, GVP, internal policies and SOPs Compliance
    Please make sure to read the attached full job description.

Must Haves

  • Minimum 3 to 5 years of relevant experience in international clinical project management
  • Experience working with studies in all phases and experience in evidence generation 
  • Oncology experience
  • Education: minimum Bachelor level ideally in Natural/Life Sciences (please note Business Administration plus relevant experience is considered)

Nice to Haves

  • Experience in Breast Cancer and/or Gynecology

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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