Associate Clinical Project Manager
1 day left
- Company
- CK Clinical
- Location
- Welwyn Garden City
- Salary
- £40ph
- Posted
- 28 Jan 2021
- Closes
- 27 Feb 2021
- Ref
- 49696
- Contact
- Stephen Lord
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
CK Clinical are recruiting for an Associate Clinical Project Manager to join a biopharmaceutical company. The role will be remote based initially, although they would want candidates to visit their site based in Welwyn Garden City, once the situation allows travel. This would be for an initial 12 month contract.
Company: This company is one of the world's largest biotech companies which is a leading provider of both cancer treatments and in vitro diagnostics.
Associate Clinical Project Manager: As a part of the Clinical Project team you will lead medical writing and editing projects for studies at phase I-III, partnering closely with key stakeholders: Clinical Science Leaders, Medical Directors, Clinical Scientists, and protocol authoring teams.
Responsibilities:
·Oversees the development of protocols, including drafting, editing, coordination of review, adjudication of review comments, and creation of project timelines.
·Acts as a key strategic thinking partner for the clinical scientist and other team members on protocol development and the above deliverables.
·Is a key strategic participant in project teams and committees.
·Acquires and demonstrates a deep understanding of needs for the clinical science organization.
Your Background:
·Strong medical writing experience to include protocol writing.
·Clinical project management experience, preferably in the biotech/Pharmaceutical industry
·Superb stakeholder management experience, able to work across cross-functional teams and members
·A proven ability to written and oral communication skills, with a proven ability to communicate effectively with all levels in the organization.
·Demonstrated experience in clinical and nonclinical document preparation and finalization.
·Demonstrated ability to collaborate and negotiate business solutions in a complex and fast-paced matrix environment.
·Team player with demonstrated strong interpersonal skills and ability to build effective working relationships throughout all levels of the organization.
·Strong analytical and problem solving skills, paired with strong partnering and performance consulting skills.
·Strong planning and organizational skills, including ability to prioritize and organize high volume workflow and follow a project through to completion, ensuring attention to detail, and highest level of accuracy within required timeframe.
Apply:
Entitlement to work in the UK is essential. Please quote reference 49696 in all correspondence.
Company: This company is one of the world's largest biotech companies which is a leading provider of both cancer treatments and in vitro diagnostics.
Associate Clinical Project Manager: As a part of the Clinical Project team you will lead medical writing and editing projects for studies at phase I-III, partnering closely with key stakeholders: Clinical Science Leaders, Medical Directors, Clinical Scientists, and protocol authoring teams.
Responsibilities:
·Oversees the development of protocols, including drafting, editing, coordination of review, adjudication of review comments, and creation of project timelines.
·Acts as a key strategic thinking partner for the clinical scientist and other team members on protocol development and the above deliverables.
·Is a key strategic participant in project teams and committees.
·Acquires and demonstrates a deep understanding of needs for the clinical science organization.
Your Background:
·Strong medical writing experience to include protocol writing.
·Clinical project management experience, preferably in the biotech/Pharmaceutical industry
·Superb stakeholder management experience, able to work across cross-functional teams and members
·A proven ability to written and oral communication skills, with a proven ability to communicate effectively with all levels in the organization.
·Demonstrated experience in clinical and nonclinical document preparation and finalization.
·Demonstrated ability to collaborate and negotiate business solutions in a complex and fast-paced matrix environment.
·Team player with demonstrated strong interpersonal skills and ability to build effective working relationships throughout all levels of the organization.
·Strong analytical and problem solving skills, paired with strong partnering and performance consulting skills.
·Strong planning and organizational skills, including ability to prioritize and organize high volume workflow and follow a project through to completion, ensuring attention to detail, and highest level of accuracy within required timeframe.
Apply:
Entitlement to work in the UK is essential. Please quote reference 49696 in all correspondence.