Study responsible Physician

Study Responsible Physician

Location: Allschwil

Duration: Contract will run until 31st December 2026

Hours: 40

Imagine your next project acting as a Study Responsible Physician for a global healthcare leader, where you will drive critical medical reviews, safety monitoring, and research projects that directly impact patient lives.

The Study Responsible Physician manages research projects and identifies opportunities for improvements to achieve business goals. This role ensures project timelines and all required project milestones are met. It also ensures assessment and selection, test method development and validation, claims support, stability protocols including preservative efficacy testing, preparation of research reports and other documentation for internal use and government submission. The successful candidate reviews and evaluates research and development protocols to ensure activities comply with industry, company and regulatory expectations for safety, efficacy and compatibility with standard clinical practice. Additionally, this position provides for scientific direction and leadership of research and development activities in support of selected product development projects, while managing the work of laboratory scientists and technicians within a designated area of responsibility, and coordinating activities with external contract laboratories and manufacturing sites. The role involves hiring, motivating, developing, and mentoring staffs to provide employee growth, as well as presenting on programs at senior management meetings and ensuring the scientific integrity and quality of all data produced.

roles and responsibilities

• Acting as study responsible physician, performing medical review, review of adjudication listings, medical monitoring, safety monitoring.

• Manages research projects and identifies opportunities for improvements to achieve business goals.

• Ensures project timelines and all required project milestones are met.

• Ensures assessment and selection, test method development and validation, claims support, stability protocols including preservative efficacy testing, preparation of research reports and other documentation for internal use and government submission.

• Reviews and evaluates research and development protocols to ensure activities comply with industry, company and regulatory expectations for safety, efficacy and compatibility with standard clinical practice.

• Provides for scientific direction and leadership of research and development activities in support of selected product development projects.

• Manages the work of laboratory scientists and technicians within a designated area of responsibility, and coordinates activities with external contract laboratories and manufacturing sites.

• Hires, motivates, develops and mentors staffs to provide employee growth.

• Presents on programs at senior management meetings and ensures the scientific integrity and quality of all data produced.

how to succeed

• Experience and qualifications necessary to act as a study responsible physician, performing medical review, adjudication listings review, medical monitoring, and safety monitoring.

• Ability to manage research projects, identify improvements, and meet project timelines and milestones.

• Competency in ensuring assessment and selection, test method development and validation, claims support, stability protocols, and preparing research reports for internal and government submission.

• Capability to review and evaluate research and development protocols for compliance with industry, company, and regulatory expectations.

• Proven leadership and scientific direction skills for research and development activities.

• Experience managing laboratory scientists and technicians and coordinating with external contract laboratories and manufacturing sites.

• Ability to hire, motivate, develop, and mentor staff.

• Strong presentation skills for senior management meetings and a commitment to ensuring scientific integrity and data quality.

benefits

This role offers a very competitive hourly rate. This contract will run until December 31st 2026

you are welcome here

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.

application process

We are looking to process the first round of applications within the next 2 working days. We do not accept applications via email or LinkedIn InMail - you must apply direct to this advert.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.