Study Clinician

Integrated Resources Inc.; Collegeville (PA); On-site; USD 70,000 - 95,000; Full time

Job summary

A leading staffing firm is seeking a Clinical Trial Team Member to collaborate on implementing clinical protocols. This mid-level role demands 5+ years of experience in trial execution and excellent communication skills to build relationships with clinical sites. The position focuses on optimizing the startup phase to ensure efficient trial completion.

Qualifications

• 5+ years experience in clinical trial execution.
• Thorough understanding of clinical trial regulations.
• Excellent communication skills with PIs and Study Coordinators.

Responsibilities

• Collaborate with study team members to implement clinical protocols.
• Communicate with sites regarding protocol requirements and recruitment.
• Manage challenges and ensure site readiness for screening subjects.

Skills

Communication

Problem-Solving

Education

BA/BS or Higher Degree

Job description

A Few Words About UsIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

This is Direct Hire Position with one of our Clients (7 to 10 Years of Total Experience)

Job Description

• Responsible for working collaboratively with the Lead Study Clinician, Clinical Operations Study Team Lead (COSTL), and other members of the Study Team (e.g. Alliance Partner/ CRO ,Regulatory Affairs, Legal, Pharm Sci, Contracts and Outsourcing) to implement one or more clinical protocols, with focus on study start-up and recruitment phases.

• Will be an integral study team member and key member of study feasibility team to identify, evaluate and select clinical sites and investigators.

• May be responsible for developing a site back-up plan that can be executed to support agreed timelines for study completion.

• Primary focus will be site communication to ensure site is knowledgeable on protocol requirements, recruitment and retention planning, solution and relationship building during the study start-up phase to optimize completion time for the clinical trial start-up phase and ensure site is ready to screen subjects immediately after initiation occurs. Work closely with sites to proactively identify, manage and timely resolve study start-up up challenges, bottlenecks, site concerns.

Qualifications

• Mid-level - Prefer ~5+ years ‘experience in clinical trial execution .

• Must have thorough understanding local and international regulations applicable to clinical trials.

• The candidate experience should not solely be operational but rather have experience in alignment with our current Clinician position roles and responsibilities .

• The candidate must have EXCELLENT communication skills and be thoroughly comfortable in speaking with prospective PIs and Study Coordinators.

• Must be proficient in collaborative problem-solving skills (A prior CRA or someone with Study Coordinator experience would be a good fit for this position.)

• BA/BS or Higher Degree preferred (M.S/PhD/PharmD/MD)

• 4-7 years of experience in Good Clinical Practices (GCP)

• 4-7 years of experience in Clinical Trials Safety Reporting