Sub- Investigator- Clinical Research Coordinator

Found in: Appcast Linkedin GBL C2 - 3 weeks ago

Lancaster, United States Chemidox Clinical Trials Full time

Job Description:

We are seeking a highly motivated and experienced Foreign Medical Doctor to join our clinical research site. The successful candidate will play a key role in both patient enrollment and business development activities. This position requires onsite attendance, is not remote.

Key Responsibilities

Patient Enrollment:

  • Utilize medical expertise to screen and enroll eligible patients into clinical research studies.
  • Conduct thorough medical assessments and ensure compliance with study protocols.
  • Collaborate with the research team to ensure efficient patient recruitment and retention.

Business Development:

  • Identify and establish relationships with potential sponsors, including pharmaceutical, biotechnology, and medical device companies.
  • Actively participate in business development activities, including attending conferences, networking events, and client meetings.
  • Assist in the development of proposals and presentations for potential sponsors, highlighting the clinical research site's capabilities and expertise.

Medical Expertise:

  • Provide medical oversight and guidance throughout the duration of clinical research studies.
  • Review study protocols and provide input on medical aspects to ensure patient safety and protocol adherence.
  • Serve as a medical resource for the research team and sponsors, offering clinical expertise and guidance as needed.

Documentation and Compliance:

  • Ensure accurate and timely documentation of patient assessments, medical histories, and study-related data.
  • Maintain compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, study protocols, and any assigned tasks.

This role may include CRC related duties which includes, maintaining regular communication with the sponsor, or IRB, assisting the investigator with budgeting and contracts, problem-solving, coordinating sponsor or regulatory audits, recruiting new studies, and professionally representing the site to all in the best possible light.

Qualifications:

  • Medical degree (MD or equivalent) from a recognized institution.
  • Prior experience working in clinical research or a related field preferred.
  • Strong understanding of clinical trial processes and regulations.
  • Excellent communication and interpersonal skills.
  • Proven ability to work effectively in a multidisciplinary team environment.
  • Proficiency in English (additional languages are a plus).

Benefits:

  • 401 (K)
  • Dental insurance
  • Health insurance
  • Bonus


Application Process: Please submit your resume and cover letter detailing your qualifications and interest in the position to hr@chemidox.com


Equal Opportunity Employer: Chemidox Clinical Trials is an equal opportunity employer and values diversity in the workplace. We encourage applicants of all backgrounds to apply.

Schedule 8-hour shift

Work Location: on-site.

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