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Freelance Clinical Research Associate , Germany - L

Employer
ClinChoice
Location
Germany
Salary
Competitive
Start date
12 Aug 2022
Closing date
25 Aug 2022

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Discipline
Clinical Research
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)

Job Details

Description:
Location: Germany - home/office based

Schedule: Contract - Part-Time

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds....

TalentSource Life Sciences (the sponsor-dedicated division of CROMSOURCE), is searching for a Freelance Clinical Research Associate to work with one of our partner companies. This is a home-based opportunity up to approximately 0.5 FTE.

CROMSOURCE is an international CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with their client counterparts.

The CRA will work closely with the Clinical Operations team in assisting with study sites and site activation, patient recruitment, study monitoring, case report form development, and study management. The person in this position will interface with site coordinators, field clinical staff, Clinical Research Organizations (CROs), and other company representatives.

Main Job Tasks and Responsibilities:
  • Participate in planning, prioritizing, and executing all aspects of Phase 1-4 clinical trials
  • Participate in problem-solving and risk mitigation strategies
  • Drafts and/or coordinates review of protocols, informed consents, case report forms, and monitoring plans
  • Interfaces with individuals in other functional areas to address routine study issues
  • Ability to develop tools and processes that increase measured efficiencies of the project
  • Assists in CRO or vendor selection
  • Participate in departmental and corporate initiatives under general supervision
  • Perform co-monitoring visits to provide oversight during site qualification, site initiation, routine monitoring, and close-out visits, as required
  • Review reports and metrics to ensure site compliance with the protocol and regulatory requirements
  • Generate and maintain reports, listings, and trackers as needed
  • Manage and QC eTMF(s) for supporting study(ies)
  • Manage study vendors to ensure compliance with the protocol
  • Complete other responsibilities as assigned


Education and Experience:
  • Bachelor's degree in life sciences or equivalent experience
  • Minimum 3+ years of experience in a clinical research environment
  • Site monitoring experience at clinical sites is highly preferred
  • Working knowledge of GCP, ICH, and relevant CFRs is required
  • Ability to work independently and manage multiple projects with minimal supervision
  • Strong communication skills, both written and oral
  • Demonstrate problem-solving skills, a strong sense of urgency, keen attention to detail, and the ability to plan, organize and successfully execute in an environment under time and resource pressures
  • Ability and willingness to travel 10 - 20% (domestic and international) as/if necessary
  • Enjoy working in a fast-paced, small-company, virtual environment


The Application Process

Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/jobs please contact careers@cromsource.com for more information.

Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Freelance, FL, Contract, Temporary, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated, Clinical Trials, Monitoring, Management.
Skills: Clinical Research Associate, Freelance, clinical trials, Contract, CRO, Monitoring, Outsourcing Location: Germany Share:

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Company

ClinChoice

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

 

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

 

Company info
Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom

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