Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK
Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK

Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK

Freelance 36000 - 60000 £ / year (est.) No home office possible
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Indero

At a Glance

  • Tasks: Monitor clinical studies, ensuring compliance with protocols and regulations.
  • Company: Indero is a global leader in dermatology clinical research with over 25 years of experience.
  • Benefits: Enjoy a collaborative work environment with opportunities for growth and development.
  • Why this job: Join a mid-sized CRO where your contributions are valued and make a real impact.
  • Qualifications: B.Sc. in a relevant field and 3 years of clinical monitoring experience required.
  • Other info: Remote work options available; travel to research sites approximately 65% of the time.

The predicted salary is between 36000 - 60000 £ per year.

Description

Contractual CRA with experience in Dermatology

The Contractual Clinical Research Associate (cCRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

This role will be perfect for you if:

  • You are an experienced CRA with a demonstrated ability to work autonomously to meet quality standards and deadlines
  • Focusing on dermatology and developing an expertise in this therapeutic area is interesting to you
  • You enjoy working for a mid-sized CRO where your contributions are noticed and valued

RESPONSIBILITIES

The cCRA will:

  • Conducts site qualification, initiation, monitoring, and close-out visits for research sites according to the monitoring plan, Indero and sponsor SOPs, ICH/CGP guidelines and applicable regulations
  • Participates in investigators\’ meetings
  • Prepares site visit reports and follow-up letters to the investigator
  • Builds productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targets
  • Performs source data verification, ensures on-site study drug storage, dispensing, and accountability, data collection, and regulatory document collection is adequate
  • Employee may be assigned to other responsibilities that do not pertain to their former description, if they have the required experience, are qualified and/or have received adequate training

Requirements

Education

  • B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience

Experience

  • 3 years of experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry
  • At least 1 year of experience in dermatology

Knowledge and skills

  • Good knowledge of ICH/GCP standards and applicable regulatory requirements
  • Strong verbal and written communication skills in English
  • Ability to prioritize different assignments and work under pressure while maintaining attention to detail and meeting timelines
  • Excellent judgement and problem-solving skills
  • Travel to research sites approximately 65% of the time
  • Excellent knowledge of Microsoft Office (i.e., Word, Excel, PowerPoint)
  • Experience in dermatology is an asset

Our company

The work environment

At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

Recruitment process: what to expect

  • As part of the recruitment process for this position you will meet various team members at Indero
  • The first interview will be conducted by Teams (30 minutes) and the second via video conference (1 hour)

About Indero

A Global Clinical Leader In Dermatology!

Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.

Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years\’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, Indero is the ideal CRO partner for clinical needs at global scale.

Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

Indero only accepts applicants who can legally work in UK. #J-18808-Ljbffr

Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK employer: Indero

Indero is an exceptional employer for Clinical Research Associates, offering a collaborative and innovative work culture where your contributions are valued. With a strong focus on dermatology and rheumatology, employees benefit from attractive advancement opportunities and the chance to work alongside brilliant colleagues in a stimulating environment. The company's commitment to equitable treatment and professional growth makes it an ideal place for those seeking meaningful and rewarding employment in clinical research.
Indero

Contact Detail:

Indero Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK

✨Tip Number 1

Familiarise yourself with the latest ICH-GCP guidelines and regulatory requirements specific to dermatology. This knowledge will not only help you during interviews but also demonstrate your commitment to maintaining high standards in clinical research.

✨Tip Number 2

Network with professionals in the dermatology field, especially those who work at CROs. Attend relevant conferences or webinars to connect with potential colleagues and learn about industry trends that could give you an edge.

✨Tip Number 3

Prepare for your interviews by practising common CRA interview questions, particularly those related to site monitoring and patient recruitment strategies. Being able to articulate your experience clearly will set you apart from other candidates.

✨Tip Number 4

Showcase your problem-solving skills by preparing examples of challenges you've faced in previous roles and how you overcame them. This will highlight your ability to work autonomously and meet quality standards under pressure.

We think you need these skills to ace Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK

Clinical Monitoring
Knowledge of ICH/GCP Standards
Regulatory Compliance
Site Qualification and Initiation
Source Data Verification
Attention to Detail
Strong Verbal and Written Communication Skills
Problem-Solving Skills
Time Management
Ability to Work Autonomously
Relationship Building with Investigators
Microsoft Office Proficiency
Experience in Dermatology
Adaptability to Changing Environments

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical research, particularly in dermatology. Emphasise relevant skills such as monitoring, data verification, and knowledge of ICH-GCP standards.

Craft a Strong Cover Letter: Write a cover letter that showcases your passion for dermatology and your ability to work autonomously. Mention specific experiences that demonstrate your problem-solving skills and attention to detail.

Highlight Relevant Experience: In your application, clearly outline your 3 years of clinical monitoring experience and at least 1 year in dermatology. Use bullet points to make this information easy to read and impactful.

Prepare for Interviews: Research Indero and prepare to discuss how your values align with theirs. Be ready to provide examples of how you've successfully managed multiple assignments under pressure in previous roles.

How to prepare for a job interview at Indero

✨Showcase Your Experience

Make sure to highlight your previous experience as a Clinical Research Associate, especially in dermatology. Be prepared to discuss specific projects you've worked on and how you ensured compliance with ICH-GCP standards.

✨Demonstrate Problem-Solving Skills

During the interview, be ready to provide examples of challenges you've faced in clinical trials and how you resolved them. This will showcase your judgement and problem-solving abilities, which are crucial for this role.

✨Familiarise Yourself with Indero

Research Indero's values and recent projects in dermatology and rheumatology. Understanding their mission and how you can contribute will help you align your answers with what they are looking for in a candidate.

✨Prepare Questions

Have a list of thoughtful questions ready to ask at the end of the interview. This shows your interest in the role and helps you assess if the company culture and work environment are a good fit for you.

Freelance / Contractual Clinical Research Associate (cCRA), Dermatology & Rheumatology CRO, UK
Indero
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