Clinical Studies Specialist

PSG Global Solutions; Illinois City (IL); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading clinical research organization in Illinois is seeking candidates to join their clinical team. The role involves conducting Phase I-IV studies, ensuring compliance with regulations, and supporting document management. The ideal candidate will have a Bachelor’s degree and experience in the pharmaceutical field, alongside strong documentation and organizational skills. The position offers opportunities for career development in a collaborative environment.

Qualifications

• Bachelor’s degree required.
• Pharma experience or professional equivalent is required.
• Ideal candidates will possess strong organizational capabilities.

Responsibilities

• Conduct Phase I-IV studies according to Federal Regulations and ICH guidelines.
• Support clinical team with organizing and filing study documents.
• Assist Clinical Team members with data queries and record reconciliation.

Skills

Strong documentation or research experience

Ability to prioritize multiple tasks

Strong organizational capabilities

Strong interpersonal skills

Excellent written and verbal skills

Education

Bachelor’s degree

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 recognizing 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

• Member of the clinical team responsible for conducting Phase I-IV studies according to Federal Regulations and ICH guidelines.
• Support clinical team, primarily in tracking, organizing and filing Phase I-IV study documents according to Federal Regulations and ICH guidelines.
• Assist Clinical Team members in handling data queries, drug inventories, study invoice payments, enrollment tracking, and record reconciliation with site documents.
• Assists the CRAs with organizing and planning study investigator meetings.
• Ensure documents are compliant with SOPs and regulatory requirements.
• Review essential/critical documents for completeness and accuracy.

Qualifications

• A Bachelor’s degree is required.
• Pharma experience or professional equivalent is required.
• Strong documentation or research experience
• Multiple TAs. Ability to manage clinical documents for multi-site studies.
• Ability to prioritize multiple tasks and/or projects with limited supervision.
• Ideal candidates will possess strong organizational capabilities and strong interpersonal skills, excellent written and verbal skills.
• Candidates must have a stable work history.
• Foreign MD will be considered only if candidate also has clinical research experience.

Additional Information

All your information will be kept confidential.