Connecting...

Banner Default Image

Regulatory CTA Submission Manager

Location: High Wycombe Salary: £40.00 - £43.00 per hour
Sector: Pharmaceuticals Type: Contract
Contact: Matt Henocq Job Published: 9 days ago

Regulatory CTA Submission Manager

12 month contract

Ltd - £43/hour

PAYE - £32/hour

This position is responsible for managing regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 - Phase 4 spanning five therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease).

The Regulatory Clinical Trial Application submission manager has experience in regulatory CTA submission regulations, requirements and will be responsible for the execution of the global CTA submission strategy, as well as the quality and completeness of the CTA regulatory submissions for Clinical Trial Applications, throughout the lifecycle of the trial.

Successful candidates for this position have: in depth regulatory submission experience and regulatory knowledge, project management and leadership skills and strong communication skills.

Responsibilities:

The Regulatory Clinical Trial Application submission manager will ensure that the required regulatory intelligence is in place to comply with country-specific requirements and will lead a cross-functional team that will compile, publish and produce Clinical Trial Authorization Applications and associated CTA lifecycle submissions (e.g., Health Authority responses, amendments, etc.).

The CTA submission manager is responsible for interactions with Health Authorities, and will be the primary contact point with regulatory authorities for communications relating to direct submissions of CTAs. The CTA submission manager ensures that key events related to the regulatory aspects of clinical trials are tracked in the company-own tracking system.

If Clinical Research Organizations are contracted to handle some (or all) aspects as outlined above, the submission manager will be responsible for liaising with and overseeing CRO staff, as required.

Required knowledge and experience:

  • Bachelor's degree required or equivalent experience; Science degree or related experience with pharmaceutical or health sciences industry is required; knowledgeable with scientific terminology.
  • Ideal candidate would possess a minimum of 8-10 years experience within regulatory affairs in the pharmaceutical industry.
  • An understanding of Drug Development, Clinical Trial Authorization Applications, Regulatory Affairs, and associated legal requirements is also required.
  • Must have strong communication skills (written and verbal), as frequent interactions with Health Authorities, Local Operating Companies, GRA, GCO, and teams occur.
  • Must have strong project management skills (e.g. planning, prioritization, management of schedules and timelines, detail orientation, strong sense of urgency).
  • Ability to lead complex projects and a high degree of problem solving capability required.
  • Must have a high level of Self-Awareness and Adaptability and strong impact and influencing skills.
  • Must have demonstrated the ability to lead multi-functional teams and build strong, productive relationships across the organization.
  • Must be able to work independently, strong initiative.

Services advertised by Gold Group are those of an Agency and/or an Employment Business.
We will contact you within the next 14 days if you are selected for interview. Privacy Policy. Equal Opportunity and Diversity Policy.

Similar Jobs

Senior Scientist - Patient Safety

Cheshire East £450 - £500 per day

Senior Scientist - Patient SafetyCheshire (WFH Initially)6 Month Contract BriefSenior Scientist - Patient Safety needed for a highly reputable Pharmaceutical organisation based in Cheshire who are looking to employ an experienced and well-rounded Senior Scientist -...

Apply

Senior Quality Supplier Manager

Macclesfield £350 - £400 per day

Senior Quality Supplier ManagerMacclesfield 12 Month Contract £400 per day BriefSenior Quality Supplier Manager needed for a leading multinational pharmaceutical organisation based in Macclesfield who are looking to employ an experienced and well-rounded Senior Qual...

Apply

Associate Director in Global Epidemiology

Cambridgeshire £550 - £650 per day

Associate Director - EpidemiologyWFH initially, 2-3 times per week in Cambridgeshire thereafter 6-month contract BriefAssociate Director - Epidemiology needed for a globally recognised Pharmaceutical organisation based in Cambridgeshire who are looking to employ an...

Apply

Associate Director Epidemiology - Immunology

Cambridge £600 - £700 per day

Job Title: Associate Director Epidemiology - Immunology Location: Cambridgeshire + Remote WorkingTerm: 12 MonthsHours: 37 Per WeekDay Rate: £600 - £700 Expected Start Date: January 2021Key Skills: Epidemiology, Design, Management, Analysis, Pharmaceutical, PhD, MSC,...

Apply

Clinical Trial Leader

Leeds £40.00 - £45.00 per hour

Clinical Trial Leader12 month contractLTD - £45/hourPAYE - £35/hourPosition duties:Serve as a Clinical Trial Leader within Ethicon Clinical Operations to execute company sponsored clinical trialsManage all operational activities of assigned clinical studiesServes as ...

Apply

Epidemiology Associate Director

Cambridgeshire £550 - £600 per day

Job Title: Epidemiology Associate Director Location: Cambridgeshire + Remote WorkingTerm: Initial 6 MonthsHours: 37 Per WeekDay Rate: £550 - £600 Key Skills: Epidemiology, Design, Management, Analysis, Pharmaceutical, PhD, MSC, Medical, Scientific, Research, Vendor ...

Apply

Evidence Delivery Associate Director

Cambridge £400 - £500 per day

Evidence Delivery Associate DirectorCambridgePharmaceuticalsInitial remote working then 3 days in the officeContract - 12 Months - £500 - £600 per day Evidence Delivery Associate Director needed for a leading Pharmaceuticals organisation based in Cambridge who are lo...

Apply

Senior Scientist / Scientist

Dublin Negotiable

My client is a growing and dynamic contract research organisation scientifically lead and evaluating novel therapeutic products on behalf of its rapidly growing client base. Attaining international recognition for its research and ability to deliver life changing the...

Apply
Linkedin_track