Clinical Trial Registries And Results Disclosure Compliance Manager
- Company
- CK Clinical
- Location
- Home-Based
- Salary
- Up to £32 PAYE
- Posted
- 03 Feb 2021
- Closes
- 05 Mar 2021
- Ref
- 49726
- Contact
- Hendre Moolman
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
CK Group are recruiting for a Clinical Trial Registries and Results Disclosure Compliance Manager to join a biopharmaceutical company on a contract basis for 6 months.
This company is a world leading pharmaceutical company that focuses on neurology and immunology. Their ambition is to transform the lives of people living with severe diseases.
Location:
Flexible remote/home working is available for this CMC Regulatory position (small molecule).
The Role:
The main purpose of the role will be to
To succeed in this role, you will come from a Life Science background with experience with clinical development, preferably trial &/or data management, biostatistics or regulatory affairs; experience in clinical trial disclosure is a plus
Quote job reference 49726
This company is a world leading pharmaceutical company that focuses on neurology and immunology. Their ambition is to transform the lives of people living with severe diseases.
Location:
Flexible remote/home working is available for this CMC Regulatory position (small molecule).
The Role:
The main purpose of the role will be to
- Support on the disclosure of trial protocol & results information on major clinical trial registries such as ClinicalTrials.gov, from disclosure planning to data entry & cross-functional review/approval to submission & release
- Keep study records on registries up-to-date at all times, and maintain complete, accurate & consistent records across internal tracking systems & archiving platforms
- Support local teams/partners by providing approved master/core disclosure content, to ensure consistency of disclosed trial information across registries worldwide
- Act as Subject Matter Expert in clinical trial disclosure, developing & maintaining effective working relationships with interfacing stakeholder groups, and providing them with relevant training & updates on clinical data disclosure & related processes
To succeed in this role, you will come from a Life Science background with experience with clinical development, preferably trial &/or data management, biostatistics or regulatory affairs; experience in clinical trial disclosure is a plus
Quote job reference 49726
Similar jobs
-
New
More searches like this
Similar jobs
-
New