Note: The job is a remote job and is open to candidates in USA. UC San Diego is a university health sciences organization supporting education, scientific research, clinical care, and community outreach. The Contract Analyst/Officer negotiates and executes clinical research agreements, primarily confidential disclosure agreements, contract amendments, and low-complexity clinical trial agreements, while ensuring compliance with university policies and applicable regulations. The role also interprets clinical protocols and budgets, monitors contract issues and approvals, maintains accurate electronic contract files, and provides support for contract intake and awards.
Responsibilities
- Using intellectual property / technology licensing / transfer concepts, and other clinical research related concepts, applies organization policies and procedures and applicable regulations to resolve a variety of intellectual property / licensing / transfer / clinical research / clinical trial contracting issues
- Works on problems and contracts of moderate scope where analysis of situations, contract language, or data requires a review of a variety of factors
- Works under direction of higher-level officer where some interpretation of established work policies and procedures is required, and, at times deviation from standard work practices may be needed
- This position works closely with both UCSD researchers / administrators and external sponsors and their representatives
- Provides excellent customer service and is proactive and resourceful in responding to inquires or resolving problems
- The primary responsibility of this role is to negotiate clear, mutually agreeable, and compliant contract terms and conditions that accurately reflect the nature and scope of the proposed research activity
- This must be done in a way that preserves the University’s relationship with the other party and is in alignment with the University’s principles and mission
- This position will primarily negotiate confidential disclosure agreements and contract amendments of varying complexity, and low complexity clinical trial agreements but will provide contract negotiation support for all agreement types, as needed
- In connection with redlining contracts, this position will monitor and document related contract issues, escalations, and required compliance reviews and approvals (e.g. Conflict of Interest, Institutional Review Board, Export Control)
- As a result, this person will have the ability to interpret and apply a variety of information and documents, including clinical protocols and clinical study budgets
- Acts as a careful data / record steward and is mindful of data / record integrity and maintains an accurate and up-to-date electronic contract file
- This position may also assist with contract intake and award related duties, and other administrative tasks, as needed
Skills
- **You are required to submit a cover letter in order for your application to be considered complete.**
- Six years of related experience, education/training, OR a Bachelor's degree in related area plus two years of related experience/training
- Working knowledge of and application of standard principles, theories and concepts such as laws, regulations, and practices pertaining to the protection and management of intellectual property, university technology transfer, and general scientific and / or technical skills in subject matter area. Working knowledge of or the ability to develop working knowledge of regulations related to clinical trials and human subjects research
- Ability to market technology to industrial partners; knowledge of contracts and grants preferred
- Working knowledge of or the ability to develop working knowledge of human subjects research policies, compliance requirements, and operations in a university, hospital, or similar setting preferred
- Ability to (i) develop working knowledge in these areas and (ii) provide advice to UCSD faculty, staff, and research administrators on industry contracting standards and procedures
- Aptitude for or demonstrated skill in communication, concise writing, and the ability to persuade, both in writing and orally
- Ability to timely and adeptly manage a high volume of transactions
- Demonstrated ability to interpret and apply laws, regulations, or written policies and procedures, and articulate or apply such in a written work product
- Ability to read, understand, and interpret clinical protocols and other medical, technical, and financial information
- Ability to read, understand, and interpret clinical trial budgets and related financial/payments language and administrative concepts. Ability to perform simple to moderately complex financial calculations, including the calculation of direct and indirect costs
- Demonstrated ability to exercise tact and discretion, be resourceful, and maintain a professional and positive attitude while under pressure
- Excellent attention to detail with strong writing, proofreading (editing, composition, spelling, grammar, punctuation), and organizational skills. Writing is clear, concise, logical, and grammatically correct. Strong skills in editing and formatting of documents
- Strong customer service skills with demonstrated ability to follow instruction, take direction well, and support team success
- Expert computer skills (including a fast typing speed), with demonstrated experience using the Microsoft Suite of programs (Word, Excel, PowerPoint, Outlook), including experience with the track changes function in MS Word, familiarity with Adobe, and the ability to adeptly work in a paper free environment using electronic systems and databases
- Demonstrated critical thinking and problem-solving skills. Ability to analyze situations, contract language, or data that requires the review of a variety of factors
- Ability to communicate clearly and interact professionally with internal and external parties. Strong interpersonal skills
- JD or other advanced degree (e.g. MS Public Health, MBA) or Paralegal or some legal / contract / research education, training, or experience preferred
Benefits
- This position has the option to work remote or hybrid schedule which includes a combination of working both onsite in La Jolla and remote. If remote, there is an expectation to attend on-site meetings a few times per year in San Diego, CA.
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