Senior Clinical Research Associate - Rare Disease - East Coast (Remote)

Worldwide Clinical Trials; United States; Remote; USD 100,000 - 125,000; Full time

Job summary

Join a leading clinical trials company as a Senior Clinical Research Associate, focusing on rare diseases. You'll manage site research activities, conduct study initiatives, and ensure compliance in a supportive and innovative environment, contributing to meaningful advances in patient care. Enjoy a stable career path with extensive development opportunities.

Benefits

Medical insurance

Vision insurance

401(k)

Disability insurance

Qualifications

• 5+ years of experience as a Clinical Research Associate.
• Experience in Rare Disease required; Nephropathy/Cystic Fibrosis experience is a plus.
• Willingness to travel required.

Responsibilities

• Manage research activities at clinical sites.
• Conduct study initiation visits (SIVs) and ensure compliance with regulatory requirements.
• Perform site start-up activities and training.

Skills

Excellent interpersonal skills

Organizational skills

Ability to work independently

Proficiency in Microsoft Office

Proficiency in CTMS

Proficiency in EDC Systems

Education

4-year university degree or RN/BSN in Nursing

Job description

Senior Clinical Research Associate - Rare Disease - East Coast (Remote)

Join to apply for the Senior Clinical Research Associate - Rare Disease - East Coast (Remote) role at Worldwide Clinical Trials

Senior Clinical Research Associate - Rare Disease - East Coast (Remote)

Join to apply for the Senior Clinical Research Associate - Rare Disease - East Coast (Remote) role at Worldwide Clinical Trials

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Team Lead, Talent Acquisition at Worldwide Clinical Trials

What Clinical Operations does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.

We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!

What you will do

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies
• Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
• Conduct study initiation visits (SIVs)
• While most of the site management efforts will be performed remotely, will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

What you will bring to the role

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to details
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS and EDC Systems

Your experience

• 5+ years of experience as a Clinical Research Associate
• 4-year university degree or RN/BSN in Nursing
• Experience in Rare Disease is required, experience in Nephropathy and/or Cystic Fibrosis a plus
• Willingness to travel required

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, General Business, and Health Care Provider

• Industries

  Research Services, Pharmaceutical Manufacturing, and Biotechnology Research

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

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