Location: Switzerland
Salary dependent on experience. Offering an extensive benefits
package.
Permanent position
Job reference: JO-**Apply on the website**
Clinical Professional are collaborating with a global pharmaceutical
organisation to recruit a Regulatory Associate Director. In this role
you will be responsible for the strategies and expertise of an
established products portfolio in Europe, duties include;
Lead Europe region submissions and represents as needed at project
team
Ensure regional regulatory lifecycle management strategy and
submission plans are executed
Collaborate with Global and Regional colleagues for the authoring of
global regulatory strategies
Lead and manage meetings with regulatory authorities and agency
meetings.
Requirements
BSc degree or equivalent in science; advanced degree preferred
Experience working on oncology product preferred
Must have worked with Centralized Procedures and have extensive
life-cycle management experience.
Knowledge of regulations and guidance governing drugs and biologics in
all phases of development, including post-marketing.
If you would like to apply for this position or discuss our other
active positions please contact Charlie on **Apply on the website**
**Apply on the website** or (Please contact us using the "Apply for
this Job Posting" box below)
If you are not currently looking but know someone who would be good
for this role then get in touch. We offer a referral scheme at
Regulatory Professionals where in which a successful recommendation
will earn you **Apply on the website** worth of vouchers *terms and
conditions apply
Regulatory Associate Director
Location: Switzerland
Salary dependent on experience. Offering an extensive benefits
package.
Permanent position
Job reference: JO-**Apply on the website**
Clinical Professional are collaborating with a global pharmaceutical
organisation to recruit a Regulatory Associate Director. In this role
you will be responsible for the strategies and expertise of an
established products portfolio in Europe, duties include;
Lead Europe region submissions and represents as needed at project
team
Ensure regional regulatory lifecycle management strategy and
submission plans are executed
Collaborate with Global and Regional colleagues for the authoring of
global regulatory strategies
Lead and manage meetings with regulatory authorities and agency
meetings.
Requirements
BSc degree or equivalent in science; advanced degree preferred
Experience working on oncology product preferred
Must have worked with Centralized Procedures and have extensive
life-cycle management experience.
Knowledge of regulations and guidance governing drugs and biologics in
all phases of development, including post-marketing.
If you would like to apply for this position or discuss our other
active positions please contact Charlie on **Apply on the website**
**Apply on the website** or (Please contact us using the "Apply for
this Job Posting" box below)
If you are not currently looking but know someone who would be good
for this role then get in touch. We offer a referral scheme at
Regulatory Professionals where in which a successful recommendation
will earn you **Apply on the website** worth of vouchers *terms and
conditions apply
We need : English (Good)
Type: Permanent
Payment:
Category: Others