Clinical Research Scientist

Progressive Recruitment; Summit (NJ); On-site; USD 70,000 - 90,000; Full time

Job summary

Une entreprise de recrutement spécialisée dans le domaine pharmaceutique recherche un rédacteur médical avec au moins 2 ans d'expérience. Le candidat idéal aura une connaissance approfondie de la recherche clinique et sera capable d'écrire des documents techniques tout en travaillant avec des équipes de développement et des autorités de réglementation. Ce poste offre une opportunité de carrière stimulante dans un environnement dynamique.

Qualifications

• Minimum 2 ans d'expérience en rédaction médicale ou technique.
• Expérience en suivi clinique préférée.
• Compréhension des essais cliniques et statistiques de base.

Responsibilities

• Assister les équipes de développement clinique et de sécurité.
• Analyser les données cliniques de sécurité.
• Collaborer avec les autorités sanitaires.

Skills

Writing

Clinical Research

Data Review

Medical Terminology

Knowledge of GCP and ICH Guidelines

Tools

Microsoft Word

Microsoft Excel

SAS

Job description

At Real, we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent, and partner with some of the world's best pharmaceutical, biotechnology, and medical companies.

As specialists in recognising talent, we pride ourselves on not just finding the best people for our client partners but also on our ability to spot the brightest talent to work for us. We are renowned for providing training and long-term career opportunities to help our employees excel, ensuring they can continue to deliver the expertise that has made Real famous.

Relationships are at the heart of everything we do, ensuring our clients and candidates continue to work with us repeatedly. This ethos shapes our business approach. We encourage and reward knowledge sharing and have various support networks and international forums to keep our employees updated on industry changes and to share local insights, delivering true global perspectives.

Job Description

• This role involves assisting the global clinical development, regulatory, and safety teams to assess and analyze clinical safety signal data, informing stakeholders to implement risk minimization strategies and proactively partnering with global health authorities.
• This position requires interaction with all areas within clinical development, medical affairs, independent review committees, and regulatory authorities to ensure timely identification, reporting, and response to safety issues.

Qualifications

• Minimum 2 years of experience in medical or technical writing
• Clinical monitoring experience preferred
• Extensive medical/scientific and clinical research knowledge
• Knowledge of Medical Terminology
• Understanding of clinical trial design, basic statistics, pharmacodynamics, and pharmacokinetics; proficient in data review and interpretation
• Experience in all aspects of drug development
• Knowledge of GCP and ICH Guidelines
• Proficiency in Microsoft Word, Excel, PowerPoint; experience with EDC databases and SAS datasets

Additional Information

All your information will be kept confidential according to EEO guidelines.

If this opportunity interests you, please call me at 646-618-8925 as soon as possible! I look forward to discussing your preferences.

If you know someone who might be interested, feel free to pass this along. I look forward to hearing from you!