Study Director/Senior Scientist in Durham

Study Director/Senior Scientist in Durham

Durham Full-Time 40000 - 50000 £ / year (est.) No working from home possible
MedPharm

At a Glance

  • Tasks: Lead and oversee scientific studies while collaborating with lab staff and project managers.
  • Company: Join a forward-thinking research organisation dedicated to innovative scientific solutions.
  • Benefits: Competitive salary, professional development, and opportunities for career advancement.
  • Other info: Dynamic role with opportunities for continuous learning and growth.
  • Why this job: Make a real impact in the science field without hands-on lab work.
  • Qualifications: Bachelor's degree in a scientific field and 3-5 years of relevant experience.

The predicted salary is between 40000 - 50000 £ per year.

NOTE: The title, Study Director, refers to the individual responsible for the scientific conduct of assigned studies and should not be interpreted as department head, manager, director, etc. While this is not a laboratory role, it is ideal for candidates who are passionate about science and want to remain closely involved without performing hands-on laboratory work.

Position Summary

A Study Director has the overall technical responsibility of a study and functions as the liaison between the laboratory staff and the Project Manager. Responsibilities include supervising and coordinating activities of client projects, identifying areas of improvement and developing new processes, leading and managing the execution of assigned studies.

Essential Functions

  • Provide strategic and technical oversight on studies.
  • Collaborate on continuous process improvement opportunities.
  • Draft study plans and contribute to the preparation of reports for sponsors.
  • Function as the Subject Matter Expert (SME) on studies, particularly on sponsor calls.
  • For any regulated studies, assure that:
    • The study protocol (plan), including any change, is approved and is followed.
    • All experimental data including observations of unanticipated responses of the test system are accurately recorded and verified.
    • Unforeseen circumstances that may affect the quality and integrity of the study are noted when they occur, and corrective action is taken and documented.
    • Test systems are as specified in the study protocol (plan).
    • Regulatory agency's (e.g. FDA, EMA, etc.) guidelines are followed where appropriate.
    • All raw data, documentation, protocols, specimens and final reports are transferred to the archives during or at the close of the study.
  • Adhere to MedPharm’s Procedures.
  • Contribute to the preparation and review of SOPs and Forms where applicable.
  • Promptly record all data according to Good Documentation Practices where applicable.
  • Review literature in preparation for studies and to regularly update knowledge by reviewing appropriate literature.
  • Supervisory Responsibilities - This position may be responsible for training, assisting or assigning tasks to others.
  • Any other duties and/or tasks that may be assigned.

Assigned Studies

The studies that a study director would be leading are pre-clinical in vitro studies conducted at the MedPharm Research & Innovations site. Most of the assigned studies would include but are not limited to the following:

  • In Vitro Release Testing (IVRT)
  • In Vitro Permeation Testing (IVPT)
  • Research Biology (e.g. various biological models, IVPT on various tissue constructs, etc.)

The majority of the assigned studies will be conducted under R&D with a small percentage conducted under a regulated setting (e.g. in vitro bioequivalence).

Education and Experience

  • Bachelor’s degree in relevant scientific field (e.g. Chemistry, Biology, etc.)
  • 3-5 years of relevant experience

Knowledge, Skills, and Abilities

  • Proficiency in technical writing
  • Must be able to analyze data sets and interpret results
  • Familiarity with JMP is a plus, but not required
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint, Teams, etc.) required.

Travel Requirements

Up to 5%

Physical Demands and Work Environment

The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is occasionally required to walk; sit; climb or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Study Director/Senior Scientist in Durham employer: MedPharm

At MedPharm, we pride ourselves on fostering a collaborative and innovative work environment where passionate scientists can thrive. As a Study Director/Senior Scientist, you will have the opportunity to lead impactful pre-clinical studies while benefiting from continuous professional development and a supportive culture that values your expertise. Located at our cutting-edge Research & Innovations site, you'll be part of a team dedicated to advancing scientific knowledge and improving health outcomes.

MedPharm

Contact Details:

MedPharm Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Study Director/Senior Scientist in Durham

Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!

Tip Number 2

Prepare for those interviews by researching the company and the role inside out. We want you to be able to discuss how your skills align with their needs, especially in areas like study oversight and process improvement.

Tip Number 3

Showcase your passion for science during interviews! Talk about your experiences and how they’ve shaped your approach to study management. We love candidates who can demonstrate their enthusiasm and commitment to the field.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we’re always on the lookout for talented individuals who are ready to make an impact.

We think you need these skills to ace Study Director/Senior Scientist in Durham

Technical Oversight
Project Coordination
Process Improvement
Study Protocol Development
Subject Matter Expertise
Regulatory Compliance
Good Documentation Practices

Some tips for your application 🫡

Show Your Passion for Science:When writing your application, let your enthusiasm for science shine through! We want to see how your passion aligns with the role of Study Director and how you can contribute to our innovative projects.

Highlight Relevant Experience:Make sure to detail your relevant experience in your application. We’re looking for candidates with a solid background in scientific studies, so don’t hold back on showcasing your skills and achievements!

Be Clear and Concise:In your written application, clarity is key. We appreciate straightforward communication, so keep your language simple and to the point while still demonstrating your expertise and knowledge.

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!

How to prepare for a job interview at MedPharm

Know Your Science

Brush up on the latest trends and developments in your scientific field. Be prepared to discuss how your knowledge can contribute to the studies you'll be overseeing. This shows your passion for science and your commitment to staying updated.

Master the Study Protocols

Familiarise yourself with study protocols, especially those related to pre-clinical in vitro studies. Understand the importance of adhering to regulatory guidelines and be ready to explain how you would ensure compliance during your studies.

Showcase Your Leadership Skills

As a Study Director, you'll need to supervise and coordinate activities. Prepare examples of how you've successfully led projects or teams in the past. Highlight your ability to identify areas for improvement and implement new processes.

Technical Writing is Key

Since you'll be drafting study plans and reports, demonstrate your proficiency in technical writing. Bring samples of your previous work if possible, and be ready to discuss how you approach writing complex scientific documents.