Scientist-I

Artech Information System LLC; Spring House (PA); On-site; USD 52,000 - 78,000; Full time

Job summary

A prominent IT staffing company is seeking a Clinical Trial Support professional in Spring House, Pennsylvania. This role involves assisting with clinical trials and collaborating with various teams. Candidates should have a Bachelor’s degree in a scientific discipline or nursing and ideally 1-2 years of relevant experience. Strong organizational and communication skills are required, along with proficiency in Microsoft Office. This is an opportunity to work in a dynamic environment while supporting critical phases of clinical studies.

Qualifications

• 1-2 years relevant work experience preferred.
• Good organization skills and communication skills.
• Proficient in Microsoft Office applications.
• Good organization skills, written and verbal communication skills.
• Proven ability to plan and track deliverables and timelines.
• Able to prioritize and respond to changing business needs.
• Proficient with Microsoft Office applications: Excel, PowerPoint, Word.

Responsibilities

• Assist with monitoring and reporting of clinical trials.
• Member of the clinical Work Group for each study.
• Support monthly medical monitoring data review activities.
• Support monthly medical monitoring data review activities.
• Assist with tracking safety events and review of SAEs as appropriate.
• Assist/Coordinate activities in support of external data requests.
• Other activities as determined by study team and phase of trial.

Skills

Organization skills

Written communication

Verbal communication

Planning

Proficiency in Microsoft Office

Education

Bachelor’s degree (or equivalent)

Bachelor’s in scientific discipline or nursing

Tools

Excel

PowerPoint

Word

Internet

Job description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Responsibilities

• Assist with activities as assigned by the Clinical Scientist or Study Responsible Physician which support the monitoring and reporting of clinical trials.
• Member of the clinical Work Group (WG) for each study assigned.
• Assist with study‑specific data review activities in support of database locks.
• Support monthly medical monitoring data review activities.
• Assist with tracking of safety events, review of new SAEs, and Narrative as appropriate.
• Assist/Coordinate activities in support of external data requests
• Other activities as determined by study team and phase of trial (ie start-up, execution or close out).

Supervision: This position reports to Clinical Scientist/SRP.

Principal Relationships

• Describe the primary working relationships (internal & external) and primary interfaces.
• Clinical Team: SRP/SRSs, Clinical Scientist, MRP, GI‑Derm/Immunology VP
• Contacts Inside the Company: Integrated Data Services, Global Medical Safety, Global Clinical Operations, programming & biostatistics
• Contacts Outside the Company: vendor and CRO/ARO contacts as appropriate

Qualifications

• Bachelor’s degree (or equivalent) required and 1-2 years relevant work experience preferred.
• Bachelor’s degree in a scientific discipline or nursing preferred. Candidates with additional degrees such as Masters (or equivalent) will also be considered but not required.
• Good organization skills, good written and verbal communication skills.
• Proven ability to plan and track deliverables and timelines.
• Individual must work well in a dynamic environment and be able to prioritize and respond to changing needs of the business.
• Proficient Microsoft Office applications and use of Internet, Excel, PowerPoint, Word.