Study Manager

Ck Group; Welwyn Garden City; Hybrid; GBP 42,000 - 60,000; Full time

Job summary

Talentmark are recruiting for a Study Manager to join a leading biopharma company on a 12‑month contract. The role is hybrid, with 3 days onsite in Welwyn Garden City and 2 days at home.

You will provide operational input into protocol design and feasibility, country selection, patient centricity and data delivery plans, and you will oversee forecasting of supplies and vendor performance. A relevant degree or equivalent experience is required, with proven study management experience and

Qualifications

• Must have a degree or equivalent experience.
• Proven experience as a Study Manager in pharma/healthcare.
• Strong knowledge of drug development processes and ICH/GCP guidelines.
• Ability to thrive in fast-paced, collaborative environments.

Responsibilities

• Provide operational input into protocol design and feasibility, country selection and data delivery plans.
• Support or manage feasibility assessments to ensure countries/sites are suitable for studies.
• Oversee vendors and third-party suppliers to meet contracted scope and performance.
• Forecast and maintain supplies (including IMP) to ensure sites have necessary resources.
• Assist in identification, management and mitigation of study-related risks and issues.

Skills

Study management

Feasibility assessments

Vendor management

Regulatory knowledge

Cross-functional collaboration

Education

Bachelor's degree

Job description

Talentmark are recruiting for a Study Manager

to join a company in the pharmaceutical industry on a contract basis for 12 months,

This role is hybrid, with 3 days per week onsite in Welwyn Garden City and 2 days home working.

Company:

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Rates are dependent upon experience

• Provide operational expertise into protocol design and feasibility, country selection, patient centricity and data delivery plans in partnership with cross-functional stakeholders.
• Support or manage feasibility assessments to ensure countries and sites are selected for participation in studies.
• Ensure vendors and third-party suppliers deliver against contracted scope of work and performance expectations and adhere to all appropriate standards.
• Oversee the forecasting and maintenance of supplies (including IMP) needed to ensure sites have the necessary resources to run clinical studies.
• Assist the study team in the identification, management and mitigation of study-related risks and issues

Your Background:

• Hold a relevant degree or have equivalent working experience
• Have demonstrated strong and consistent performance as a Study Manager (or equivalent) in the pharmaceutical and/or healthcare industry.
• Possess strong working knowledge of drug development process and relevant regulations, including ICH and GCP guidelines.
• Feel comfortable thinking on your feet and thrive in fast -paced, ambiguous and highly collaborative environments.

Company:

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.