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Trainee Medical Reviewer Location: Berkshire (hybrid working model – at least 3 days on site) Duration: 12 months About the Role SRG are working closely with a top pharmaceutical company on an excellent role for aspiring Medical Affairs professionals. We are seeking a Trainee Medical Review Advisor to support the review and approval of promotional and non-promotional healthcare materials across a range of therapeutic areas. This role offers an excellent opportunity for a pharmacy or medical graduate to develop expertise in medical review, compliance, and healthcare communications, while working closely with cross-functional teams in a regulated environment. Key Responsibilities • Support the review and approval of promotional and non-promotional materials to ensure compliance with relevant industry regulations and codes of practice., • Provide scientific and compliance support to brand and cross-functional teams across multiple therapeutic areas., • Contribute to the development and implementation of compliant processes and standards for healthcare communications and activities., • Help deliver practical, compliant solutions that support business objectives, product launches, and marketing initiatives., • Review materials accurately and efficiently to meet business timelines and quality standards., • Participate in medical review projects and continuous improvement initiatives to enhance ways of working and best practices. Skills & Experience Required • Pharmacy or Medical degree (essential)., • GPhC registration for pharmacists or GMC registration for physicians (essential), • Strong ability to analyse, interpret, and communicate complex scientific, pharmacological, or medical information., • Excellent attention to detail and commitment to accuracy., • Ability to work effectively in a fast-paced, deadline-driven environment., • Strong problem-solving skills with the ability to identify issues and develop practical solutions., • Experience working within cross-functional teams is desirable. What We're Looking For • A keen interest in medical affairs, healthcare compliance, and medical review., • Motivation to develop towards Medical Signatory status., • Strong communication and stakeholder management skills., • A collaborative approach and willingness to learn in a highly regulated environment. To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on 07836 251472.

Volga Partners, a U.S.-based company, specializes in Artificial Intelligence and machine learning, catering to top technology giants and multinational corporations. Beyond that, we offer a spectrum of services including IT, business process outsourcing, advanced professional services, and crowdsourcing in both established and emerging markets. Our client is seeking candidates interested in Freelance/Task-based work for an ongoing project. The hours will align with the IST time zone. PLEASE REVIEW THE MANDATORY REQUIREMENT BEFORE APPLYING: • Must be able to read and write in English., • Must be comfortable and understand this is a task-based role. Task-Based Project Scope This is a freelance, task-based role designed for those seeking supplemental income. It’s essential to understand the nature of freelance work—tasks will be assigned as they become available, and work may be irregular or intermittent. Notifications will be sent via WhatsApp, email, or Slack (after onboarding through the client’s portal). All tasks are offered on a first-come, first-served basis, making this role ideal for individuals who are comfortable with flexible, on-demand work. POSITION We are looking for a Language Data and Quality Reviewer with proficiency in English to join our team. This role is critical in researching and analyzing data for various entities, tools, and datasets that will be introduced through on-the-job training. The ideal candidate should have a background in technology, with strong logical and analytical skills to assess data and provide valuable insights. While prior experience in similar roles is beneficial, we encourage candidates with some experience in data analysis, quality assurance, or related fields to apply, especially those looking to grow their skills in a global, dynamic work environment. Key Responsibilities • Data Interpretation: Analyze datasets, translating raw data into actionable insights that can support business improvement strategies., • Data Manipulation: Handle data batches, apply labeling techniques, and manipulate data according to project requirements, ensuring high accuracy., • Quality Assurance: Oversee the quality of training data, identify issues or anomalies, and implement corrective measures to maintain data integrity., • Language Translations: Provide translations and contextual understanding where necessary to ensure data is aligned with language and cultural nuances., • Recommendations: Offer suggestions aimed at improving business processes and outcomes based on your data analysis. Desired Qualifications • Some experience in data labeling, manipulation, or quality assurance, particularly in technology or related fields., • A proactive attitude towards continuous improvement, staying updated with new advancements in AI technologies and data analysis techniques., • Logical and analytical skills to ensure data accuracy and support project goals. Required Skills • Proficient in English., • Excellent logical reasoning and analytical skills, with the ability to interpret complex datasets and derive meaningful insights., • Experience with data labeling and manipulation techniques, ensuring accuracy and reliability in data processing., • Strong attention to detail and a proactive approach to identifying and addressing data quality issues. Required Qualifications • Proficiency (reading, writing, and/or speaking) in English., • Strong computer skills, particularly in typing and writing., • Meticulous attention to detail., • Proactive attitude with a commitment to fostering positive experiences for others., • If you are certified as a Linguist, it is considered a plus! Interview Process • Submissions are reviewed by a recruiter., • Selected candidates will be invited to complete an Applicant Response Form and may be invited to a first and final interview. Additional Requirements • Must have own device (laptop/desktop)., • Currently hiring for Freelance/Task-based (ranging from 0 to 20 hours a week!)., • Candidate must be available in IST (preferred 8am IST onwards)., • Must have access to good Wi-Fi connection during working hours., • This role is a 1099 independent contractor position., • Please note that this classification may vary based on your location and local regulations., • For most candidates outside of the US, a W-8 BEN form is provided. Onboarding & Compliance Requirements • All global contractors will be onboarded through our platform, Deel.com, to ensure alignment with international compliance standards., • Successful completion of onboarding is required to begin work, which includes submitting the necessary documentation within the specified timeline., • Candidates should be prepared to provide accurate and compliant documents according to the requirements of their region. Compensation • USD $13.00 to $14.00 per hour This is an exciting opportunity for a remote freelance position! Please kindly note that hours are dependent on the volume of tasks given by the client. Perfect for a supplemental income opportunity. We look forward to receiving your application! Mandatory Requirements • Must have reliable high-speed internet and a functioning device (laptop, desktop, etc.) to ensure seamless communication and productivity., • Urgency: Due to the nature of the role, it is essential that all candidates have these resources in place from day one to avoid any delays in onboarding or task completion.

Are you experienced in GMP manufacturing and quality documentation, with a strong eye for detail and compliance? Do you take pride in ensuring batch records are accurate, complete and audit ready? If so, this Quality Compliance Assistant role could be a opportunity? Make your application after reading the following skill and qualification requirements for this position. This Quality Compliance position is based in Petersfield. xrnqpay The working hours are Monday to Friday 7am-3pm. The role is paying a competi...

Trainee Medical Reviewer Location: Berkshire (hybrid working model - at least 3 days on site) Duration: 12 months About the Role SRG are working exclusively with a top pharmaceutical company on an excellent role for aspiring Medical Affairs professionals. We are seeking a Trainee Medical Review Advisor to support the review and approval of promotional and non-promotional healthcare materials across a range of therapeutic areas. This role offers an excellent opportunity for a pharmacy or medical graduate to develop expertise in medical review, compliance, and healthcare communications, while working closely with cross-functional teams in a regulated environment. Key Responsibilities Support the review and approval of promotional and non-promotional materials to ensure compliance with relevant industry regulations and codes of practice. Provide scientific and compliance support to brand and cross-functional teams across multiple therapeutic areas. Contribute to the development and implementation of compliant processes and standards for healthcare communications and activities. Help deliver practical, compliant solutions that support business objectives, product launches, and marketing initiatives. Review materials accurately and efficiently to meet business timelines and quality standards. Participate in medical review projects and continuous improvement initiatives to enhance ways of working and best practices.Skills & Experience Required Pharmacy or Medical degree (essential). GPhC registration for pharmacists or GMC registration for physicians (essential) Strong ability to analyse, interpret, and communicate complex scientific, pharmacological, or medical information. Excellent attention to detail and commitment to accuracy. Ability to work effectively in a fast-paced, deadline-driven environment. Strong problem-solving skills with the ability to identify issues and develop practical solutions. Experience working within cross-functional teams is desirable.What We're Looking For A keen interest in medical affairs, healthcare compliance, and medical review. Motivation to develop towards Medical Signatory status. Strong communication and stakeholder management skills. A collaborative approach and willingness to learn in a highly regulated environment.To Apply Please click and submit your profile and/or to discuss further, contact Theo Charles on (phone number removed) Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

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