Clinical Research Scientist

PSG Global Solutions; Summit (NJ); On-site; USD 70,000 - 90,000; Full time

Job summary

A global talent solutions firm in New Jersey is seeking a professional for a key role in medical writing and clinical safety. You will analyze clinical safety data and collaborate with global health authorities. A minimum of 2 years in medical or technical writing is required, along with substantial knowledge of clinical research and drug development processes. Proficiency in Microsoft Office is essential. This position provides significant opportunities for career growth and development.

Qualifications

• Minimum 2 years experience in medical or technical writing.
• Clinical monitoring experience preferred.
• Extensive knowledge in medical/scientific and clinical research.

Responsibilities

• Assist global clinical development and regulatory teams.
• Analyze clinical safety signal data and inform stakeholders regarding risk strategies.
• Interact with clinical development, medical affairs, and regulatory authorities.

Skills

Medical writing

Clinical monitoring

Medical/scientific knowledge

Knowledge of Medical Terminology

Clinical trial design

Pharmacodynamics and pharmacokinetics

Data review and interpretation

Knowledge of GCP and ICH Guidelines

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

EDC databases

SAS datasets

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 on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

• This position has a key role to assist the global clinical development, regulatory, and safety to continually assess and analyze clinical safety signal data and inform key stakeholders to implement strategies to minimize risk and proactively partner with global health authorities.
• This position includes interactions with all areas within clinical development, medical affairs, independent review committees, and regulatory authorities to ensure timely identification, reporting, and response to health authorities with regards to safety issues.

Qualifications

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

Additional Information

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

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP! I want to know more about your preferences.

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