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Senior Executive-Clinical Regulatory Writing Consultant

Mexico City, Mexico
Start date
7 Jun 2024
Closing date
7 Jul 2024

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Job Details

Senior Executive-Clinical Regulatory Writing Consultant

at ClinChoice (View all jobs)

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 Senior Executive-Clinical Regulatory Writing Consultant 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.

Main Job Tasks and Responsibilities:

The Medical Writer will research, create, edit, and coordinate the

production of clinical and regulatory submission documents, including

clinical study reports, protocols, informed consent forms etc.

The Medical Writer may provide writing support for more complex

clinical documentation, with appropriate departmental supervision.

The Medical Writer may serve as primary contact with client under

appropriate departmental supervision.

Developing efficient work plans and timelines for medical writing


Serve as quality control person for the clinical regulatory documents and

peer review clinical documents.

Ensure document content and style adheres to appropriate regulatory

guidelines and complies with departmental and corporate or client SOPs

and style guidelines,

Ensure that all work is complete and of high quality prior to team

distribution or distribution to client.

Perform literature searches/reviews as necessary to obtain background

information for development of documents.

Attend internal technical team and client team meetings as required

Keep up with professional information and trends in the writing and

regulatory industry through workshops and conferences and ensure the

appropriate transfer of that information to the department.

Participate in departmental process improvement and training initiatives.

Other assignment duties as assigned by department management.


Responsible for confidentiality, integrity, availability, and safeguarding

of data,

Responsible for reporting of security incidents and PIMS breaches as


Comply with company QMS, ISMS and PIMS requirements and

applicable regulatory requirements,

Demonstrate adherence and compliance to PIMS/GDPR requirements as

follows: processed fairly, transparently, and lawfully; collected for

specified and legitimate purposes; adequate, relevant, and limited to the

specified purposes; processed in a secure manner.

Education and Experience:

  • Pharm, M. Pharm, M.Sc. Life Sciences, PhD, Pharm D, and in alignment with

  • project / business team requirements.

    Minimum 3 to 5 years of relevant experience in identified functional domain/ business work stream.

    Specific Role Requirements and Skills:

    Looking for specific experience involves both Investigator Brochures and Clinical Overviews for labeling changes.

    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 ClinChoice

    ClinChoice 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 Ethos

    Our 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.

    Key words: Medical Writing, Clinical Medical Writing




    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
    +44 1628 566121
    Suite G48
    268 Bath Road
    SL1 4DX

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