Clinical Scientist

Immediate need for a talented Clinical Scientist. This is a 12+ Months Contract opportunity with long-term potential and is located in U.S.(Remote). Please review the job description below and contact me ASAP if you are interested.

Job ID:24-22426

Pay Range: $70 - $85/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• The clinical scientist will be a responsible member of a clinical team dedicated to the development and execution of clinical strategies and the clinical and operational implementation of a complex compound program.
• This individual will provide active scientific contribution to a cross-functional clinical team developing a molecular entity, provide input to the clinical development plan, work on the development of the clinical trial protocol, clinical trial materials, and take responsibility for coordinating completion of clinical study reports and support preparation of relevant documents for regulatory filings.
• This role will involve extensive team matrix interactions with colleagues from a number of different disciplines with particular collaboration with clinical operations.
• This individual may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area.

Key Requirements and Technology Experience:

• Ophthalmology/retina clinical development and clinical operations experience required
• Scientific expertise or interest and ability to learn in the domain of assigned study/project.
• Well organized, high level of autonomy and motivation,
• Leadership to give directions and organize the activities on behalf of the CRD
• Quality focused, able to develop good practices, using a critical data-driven and risk management approach
• Familiar with digital tools such as data analytics or agility to use them
• Good communication skills (verbal and written)
• Multiple tasks handling and prioritization
• Ability to synthesize the information, good presentation skills
• Ability to work autonomously and to efficiently provide status reports
• Ability to anticipate and timely escalate issues and to execute action plans
• Team and results oriented
• Experience of working internationally with Strong English skills (verbal and written if English is not the native language)
• This position may require approximately 10% travel (within the US) to visit clinical sites.
• 10% will be required for clinical site management, this is clustered travel (Reimbursement will be offered).
• Must have: Ophthalmology/retina experience is required A minimum of 3 years of clinical research and clinical drug development experience within the ophthalmology/retina pharmaceutical industry or CRO is required Knowledge in ICH - GCP (Good Clinical Practices) (International Conference on Harmonization).
• Ph.D., or similar; bachelor’s or master's degree considered for candidates with experience.
• Degree in Bio Sciences/ Pharmacology Fluent in English Nice to Have: Statistical, data management, and regulatory knowledge.

Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.