Associate Consultant - UK Internship (US applicants only)

The Role

Scendea is seeking a highly motivated individual to join our global team as an Associate Consultant in a paid internship placement within our Product Development and Regulatory Consulting team. This 6-month internship, starting in July 2025, will be based at our UK Head Office and offers the opportunity to gain valuable hands-on experience. Upon successful completion of the internship, you will be eligible to transition into a permanent position at our Washington D.C. office, which is set to open in January 2026.

To be considered for this internship, you must be eligible to work in the US and willing to relocate to Washington D.C. for the permanent role after the internship concludes. This exciting opportunity is ideal for someone wanting to start or develop a career in regulatory project management, regulatory affairs and medical/scientific writing. The successful candidate will have a strong interest in facilitating the entry of Client’s compounds into clinical trials and assisting in the activities required for successful international marketing approvals.

Eligibility & Conditions

Applicants must be eligible to obtain a Temporary Worker: Government Authorised Exchange Visa to work in the UK and be able to fund their residence for the duration of the placement. Applicants must be willing to reside and work in Washington D.C. in the future, without the need for sponsorship. Further information regarding UK Internships will provided in interview or visit our LinkedIn page for more info.Closing date for applications is 9th June 2025 and candidates will be notified of the outcome of their application no later than 13th June 2025.

Requirements

Project management to ensure delivery of contracted activities, which could include direct contact with multiple clients and stakeholders.

Complete relevant tasks within scope or under supervision to ensure successful project delivery with adherence to timelines and budgets.

Support in the creation and delivery of high-quality billable related product development and regulatory-related documentation for clients.

Develop and maintain technical knowledge in the area of product development and international regulatory affairs.

Perform literature and data searches, collating and summarising data in an appropriate manner for stakeholders.

Manage project documentation within company systems.

Support and develop strategic drug development strategies in the area of regulatory affairs, Non-Clinical, Clinical, and CMC development.

Assess and analyse scientific data.

Assist in the development and maintenance of Standard Operating Procedures (SOP) and other relevant training materials.

Support the preparation of written estimates, quotations, and contracts for clients.

Be an active participant of the global team to support colleagues and the company in achieving the company goals.A high scientific calibre with a life science focused BSc (or equivalent), and a higher degree (e.g., a life science focused MSc or PhD).

Skills and Experience

A general awareness of drug development and medical/regulatory affairs is required, and prior industry experience would be advantageous.

Any experience with regards to medical/scientific writing would be a strong asset for this position.

Excellent writing skills in English – able to summarise complex scientific data, thus facilitating the review of such data by external parties.

High level of verbal communication and presentation skills in English, computer literacy, and competency in MS Office programs.

Exemplary organisational and time management skills with a high level of attention to detail, ability to balance competing priorities, and to complete work within a set timeframe.

Proven ability to work proactively, autonomously, and as part of a team.

Some experience in project management would be a significant advantage for this role. Such as managing a research project (e.g., during a PhD).

Willingness to work flexible hours and travel for short periods, sometimes at short notice, within the UK, and or internationally.

A clear ambition to progress your career in medical/scientific writing and regulatory consulting.

Commercial experience is not a prerequisite for this position.

Benefits

A competitive salary.

26 days’ holiday( pro-rate’d) plus public holidays and discretionary additional day for birthday.

Access to Employee Assistance Programme.

Employee Ownership Trust Scheme.

Coaching, mentoring and support of your continuous learning, and professional development within a highly recognised international team.