Senior Medical Writing Scientist

Publié il y a 3 jours par Johnson & Johnson

null, null

Je postule

Ajouter à ma sélection

Description du poste

Job Description

Senior Medical Writing Scientist

We are recruiting for a Senior Medical Writing Scientist to join the Medical Writing team to support our Oncology therapeutic area. The position may be located in the UK, Belgium, Switzerland, France, Germany, Spain, Netherlands, Poland or New Jersey (US). Are you ready to join our team? Then please read further!

Who is Janssen? We’re more than 30,000 people working hard to prevent, treat, cure and stop some of the most devastating and complex diseases of our time. From heart disease to HIV, Alzheimer’s disease to cancer, we are committed to issues that touch everyone’s lives. Our mission is to transform individual lives and fundamentally change the way diseases are managed, interpreted, and prevented. We believe that challenging something is the best way to change it. So every day, in more than 150 countries, we bring ground breaking science and the most creative minds in the industry together to think differently about diseases. We aim not only to innovate but also to empower people with the tools they need to make informed decisions and achieve the best possible results for their health.

Key Responsibilities:

Depending on the experience and level of the appointed position, your responsibilities will cover a range of activities including:

Prepare and finalise clinical documents such as, but not limited to, clinical study reports, investigator’s brochures, protocols, summary documents, risk management plans, and regulatory responses.

Participate in or lead cross-functional document planning and review meetings. Interact with peer writers and colleagues from other departments. Able to lead program-level writing teams with supervision.

Coach or mentor more junior writers on document planning, processes, content.

If a lead writer for a program: Primary point of contact and champion for medical writing activities for the clinical team. Responsible for planning and leading the writing group for assigned program.

Establish document timelines and strategies in accordance with internal processes, with mentorship from functional management and clinical team, as needed.

Acquire, maintain, and apply knowledge of the industry, company, and regulatory guidelines.

Qualifications

University/college degree required. Masters or PhD preferred.

Experience and Skills:

We would value a colleague with these qualities:

Experience within pharmaceutical/scientific environment preferably with relevant medical writing experience.

Ability to learn and recognise how to best interpret, summarise, and present statistical and medical information to ensure quality and accuracy of content in document types under supervision.

Attention to detail.

Strong oral and written communication skills.

Leadership skills, both in time management as well as in project/process management.

Able to resolve basic problems independently and complex problems under supervision.

Demonstrate learning agility.

Able to build solid and positive relationships with cross‐functional team members.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Il y a 3 jours

Je postule