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Enhancing and supporting life science companies on their journey to develop next generation medicines.

Excellence 

Accountability 

Creativity 

Respect 

Integrity 

Equality 

Teamwork 

Innovation 

We work in fast-moving evidence-driven teams

WORKING HERE

Adnovate is a fast-growing, results-driven clinical development consultancy that is looking for talented and motivated people from a wide range of backgrounds to join the team. We pride ourselves on creating a work environment that is diverse, inclusive, supportive and welcoming, enabling employees to achieve their full potential. We recognize the importance of flexibility to optimize work-life balance and use remote working to help employees meet the needs of their families and loved ones.

We care about our staff and their career ambitions

OUR VALUES

Adnovate is built around the core principles of innovation, and evidence-based science and medicine. We strive to work in the best interests of our clients, consistently producing high-quality deliverables and developing relationships based on trust, honesty and integrity. We promote continuous learning and development of technical and leadership skills. Our working environment is one of mutual respect and accountability within high-performing teams of industry-seasoned experts.

“Despite huge innovation in the drug development sector, many diseases and medical conditions still do not have adequate therapies. Drug development is a high-risk business with many companies failing to advance their approaches. In some cases, having access to seasoned professionals with functional expertise to optimize the development of their assets would have improved the chances of successful outcomes. Joining Adnovate will give you a chance to work with industry experts and help life science organizations to develop the next generation of medicines for the benefit of patients.”

Ajay DuggalFounder & Managing Director

Joining Adnovate gives you the opportunity to work as a valued member of our team, contributing to drug discovery and development with the goal of improving healthcare outcomes at a population level. If you enjoy the challenge of working in a high-performance, results-driven environment with experts from around the world, Adnovate is the place for you!

September 11, 2023
445 DAYS LEFT TO APPLY
Scientific Project Lead
Remote
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Full Time
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Immediately
We are looking for a translational and/or clinical development scientist/strategist (MD/PhD) who will be responsible for the scientific and technical leadership of assigned consulting projects and project teams. The Scientific Project Lead is responsible for ensuring the scientific validity and excellence of projects, and the delivery of client-focused outputs of the highest quality. The role demands a flexible approach adapted to the specific and evolving needs of our clients and their assets in development.

Responsibilities

  • Primary point of contact to the client ensuring scientific validity and excellence within the approved budget, as well as scientific and technical leadership to the team assigned to work on the project. 
  • Identify and successfully integrate appropriate team members for the project, ensuring an integrated and seamless Adnovate experience for the client and the quality of deliverables on time and in budget. 
  • Ensure teams roles and responsibilities and time allocations are appropriately communicated and agreed and individuals are motivated to perform.
  • Plan for and document internal team and external client meetings cross-functionally to ensure the successful execution of the project, effectively communicating with and gaining buy in from all levels. This includes regular meetings with the client’s primary point of contact, coordination of client communications to ensure that all expectations are being met, quickly and effectively addressing any needs or concerns, and escalating any issues to senior management, as appropriate. 
  • Ensure project plans and powerpoint presentations (with summary slides to clearly present ideas, plans and timelines at an appropriate level for the project and suitable for C-suite and Board communications) are prepared by the team in timely fashion and to the highest standards for presentation style and grammar, including back up slides to capture all work conducted by the team. 
  • Become subject matter expert for the asset and all technical aspects of the project through reading key documents including literature and the work of the Adnovate team. 
  • Identify emerging client needs and formulate appropriate solutions to meet the regulatory (including ICH GCP), strategic and operational needs of the project, mitigating risks and meeting revenue, profitability and client satisfaction objectives.
  • Identify potential opportunities to expand the collaboration with the client cross-functionally. Proactively alert changes in scope and support the timely implementation of change orders as necessary.
  • Build and maintain successful long-term relationships with the client. 
  • Ensure company and business unit policies, standards, and procedures are met.

Qualifications

  • Advanced degree (PhD and/or MD) in a life sciences discipline.
  • Typically requires at least 10 years of industry experience in clinical development, including at least 5 years of consulting and project management.

Skills

  • Comfortable presenting and interfacing with internal and client senior executives, investors, regulators/policy makers.
  • Thorough understanding of the biopharmaceutical R&D process in combination with solid business acumen and an appreciation of the broader business issues.
  • Strong grammatical/technical-writing, oral communication and presentation skills, excellent use of the English language. Proficient with Excel, Word and Powerpoint.
  • Able to work effectively and flexibly to deadlines in a demanding, challenging, rapidly changing environment. Curious, collaborative, pragmatic, entrepreneurial and self-motivated, without the need for significant infrastructure and support, and with an understanding of the dynamics of high-growth companies.
  • Strong interpersonal skills with the ability to gain respect of and influence senior management team, clients and personnel at all levels.
  • Demonstrated understanding of the client decision-making processes and constraints.
  • Strategic thinker, strong problem-solving and analytical skills, and the ability to execute in complex situations at the tactical level.
September 4, 2023
445 DAYS LEFT TO APPLY
Medical Writer
Remote
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Full Time
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Immediately
We are hiring a seasoned Medical Writer with broad industry experience producing high-quality documents for clinical research. You will operate as the lead writer and primary client contact, often managing contributions from multiple writers working on related documents. This is a remote position with minimal travel requirements.

Responsibilities

  • Write/QC clinical documents for submission to regulatory authorities, including but not limited to; briefing documents; investigator brochures; study protocols; informed consent forms; interim and final clinical study reports; safety update/aggregate reports; common technical document (CTD) clinical overviews and summaries; and integrated summaries of safety and efficacy. Write client-sponsored manuscripts. Ensure that all work is completed to the highest quality.
  • Lead writing activities for clinical development programs and act as primary client contact. Manage the scope of work, delegation of responsibilities, strategic planning and timelines, workplans, technical information, and input from clients and other team members throughout the program. Enable the team to work efficiently and effectively to meet milestones and achieve team objectives.
  • Participate in the creation, identification and leveraging of new business opportunities, support new business proposals and bid defences as required. Build and maintain successful long-term relationships with clients.
  • Ensure company and business unit policies, standards, and procedures are met. Keep abreast with regulatory and industry requirements, guidelines, and trends.

Qualifications

  • Advanced degree in a life sciences discipline.
  • Typically requires at least 10 years of industry experience as a medical writer.

Skills

  • Comfortable presenting and interfacing with internal and client executives.
  • Thorough understanding of the biopharmaceutical R&D process in combination with business /consulting acumen.
  • Strong grammatical/technical-writing, oral communication and presentation skills, excellent use of the English language. Proficient with Excel, Word and PowerPoint.
  • Able to work effectively and flexibly to deadlines in a demanding, challenging, rapidly changing environment. Curious, collaborative, pragmatic, entrepreneurial and self-motivated, without the need for significant infrastructure and support, and with an understanding of the dynamics of high-growth companies.
  • Strong interpersonal skills with the ability to gain respect of and influence internal and external clients.
  • Demonstrated understanding of the client decision-making processes and constraints.
  • Strategic thinker, excellent organization, time management and multi-tasking capabilities, strong problem-solving and analytical skills. Good attention to detail and the ability to execute in client situations at the tactical level.

Are you ready to join our team?

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