Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Regulatory Affairs Associate Consultant for 12 months Contract with possibility of extension to join one of our clients.
ClinChoice is a global full-service 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 the client’s counterparts.
Responsibilities
· Accountable for aligned markets for required regulatory in-scope ancillaries and samples
· Understand aligned markets regulatory ancillary requirements
· Manage aligned markets ancillary and samples requests are completed per agreed timelines in support of planned regulatory submissions
· Manage in a matrix environment with effective communication across multiple functions
· Escalate to Client and Contractor point of contact when timelines may not be reached.
· Maintain Clients systems and process throughout processing of request to ensure real time reflection of request is visible to all users.
Minimum requirements
- 3+ years Regulatory experience
- Demonstrated ability to support international product approval
- Demonstrates ability to work within a demanding environment with a strong focus on quality and timelines.
- Proven technical aptitude and ability to quickly learn and apply new software, regulations and quality standards.
- Can demonstrate leadership and team skills.
- Advanced Microsoft Office Suite skills.
- Highly efficient communicator.
- Acts decisively and seizes accountability
- Bachelor’s degree Level (desirable or equivalent work experience.
- Familiarity with pharmaceutical organizational Structures.
- The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for 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.
Who will you be working for?
About ClinChoiceClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company EthosOur mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
#LI-PB1 #LI-Remote #Contract
Skills Required
- 3+ years of regulatory experience
- Experience supporting international product approval
- Ability to work in a demanding environment with strong focus on quality and timelines
- Technical aptitude and ability to quickly learn and apply new software, regulations, and quality standards
- Leadership and team skills
- Advanced Microsoft Office Suite skills
- Highly efficient communication skills
- Ability to act decisively and take accountability
- Bachelor's degree or equivalent work experience
- Familiarity with pharmaceutical organizational structures
ClinChoice Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.
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Flexible Benefits — Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
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Leave & Time Off Breadth — Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
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Healthcare Strength — Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.
ClinChoice Insights
What We Do
ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.
