Clinical Trials Technology Transfer & Agreements Manager

Kelly; Washington (District of Columbia); On-site; USD 30,466 - 36,493; Full time

Benefits offered by this job

Competitive compensation

Comprehensive benefit package

Vacation leave

401K plan

Job summary

A top talent solutions firm in Washington is searching for a Clinical Trials Technology Transfer & Agreements Manager to support the NIH. This temporary role (3-6 months) offers diverse responsibilities in managing agreements and projects. Candidates should possess a Master's in Biological or Life Sciences and at least three years of relevant experience. The position offers competitive compensation, comprehensive benefits, and an opportunity to work closely with clinical trials in an esteemed environment.

Qualifications

• Master’s degree in Biological Sciences or Life Sciences is required.
• Minimum of three years of experience in related fields.

Responsibilities

• Draft and negotiate Cooperative Research and Developments Agreements.
• Plan and negotiate Clinical Trial and Material Transfer Agreements.
• Provide support for data and monitoring plans.
• Maintain records of Active Agreements and project timelines.
• Coordinate with stakeholders to track financial support.

Skills

Clinical trial project management experience

Ability to problem solve

Exceptional written and oral communication skills

Ability to work independently and in a team

Familiarity with clinical trials in Oncology

Familiarity with research subcontracting

Ability to communicate with high-level personnel

Education

Master’s degree in Biological Sciences or Life Sciences

Job description

Kelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. Kelly Government Solutions offers administrative, IT, engineering, scientific, and healthcare professionals the opportunity to work with leading medical research centers, biotechnology and pharmaceutical development companies in the world. We are seeking individuals qualified to work as a Clinical Trials Technology Transfer & Agreements Manager to support the mission of the National Institutes of Health (NIH).

This is a 3-6 month Temporary role, salary $3,000 per week .

This is a long-term contract position which offers:

• Competitive compensation and comprehensive benefit package
• Optional health, vision, and dental plans
• Vacation leave as well as 10 paid federal holidays and 401K plan.
• Access to NIH’s unparalleled resources and niche scientific initiatives

Duties Include:

• Provide support for the drafting and negotiation of Cooperative Research and Developments Agreements for NCI scientists and their industrial/academic research partners.
• Provide support for the planning and negotiation of Material Transfer Agreements (MTAs), Clinical Trial Agreements (CTAs) and other technology transfer agreements.
• Liaise with MATCH stakeholders, both internal and external.
• Provide support to staff in ensuring that agreements in the MATCH program are consistent with existing agreement and NCI/NIH policy.
• Provide agreement support and coordination between CDP and CTEP.
• Create data/monitoring plans and provides regular written reports detailing progress against tasks and milestones.
• As the NCI Formulary CRADA negotiations. Maintain the “Active Agreements” list on the CTEP Website of current CTEP Agents available for request.
• Collaborate with NCI and other stakeholders to implement key process improvement initiatives.
• Maintain the ACG SharePoint Page as requested. Provide scientific and administrative project management support.
• Develop a new tracking and reporting system for the Biomarkers and Medical tests funding sources. 2 Generate appropriate SOPs and workflows for the new processes.
• Monitor project risk by proactively anticipating issues and develops contingency plansand solutions. Work with the CTEP to immediately address issues as they arise.
• Monitor LOIs and protocols to make an early determination of associated correlative work funding mechanism (CRADA, MoCha, NCLN, grants, etc.).
• Collaborate with CTEP IDB, CDP and RAB staff to ensure associated correlative work is identified.
• Collaborate with internal and external stakeholders for intellectual property requirements, CRADAs, MTAs, etc. 5 Work with CTEP and contracting project management staff to ensure the operational needs of the project are being met.
• Coordinate with NCI, CRADA partners and CTEP to track timeline and pending financial support.
• Work products and documents related to providing scientific and administrative project management support
• work with CTEP and contracting project management staff to ensure the operational needs of the project are being met
• collaborate with CTEP IDB, CDP and RAB staff to ensure associated correlative work is identified.
• Ad-Hoc Work products and documents related to developing a new tracking and reporting system for the Biomarkers and Medical tests funding sources; monitor LOIs and protocols to make an early determination of associated correlative work funding mechanism (CRADA, MoCha, NCLN, grants, etc.)
• Ad-Hoc Work products and documents related to providing support for the drafting and negotiation of Cooperative Research and Developments Agreements for NCI scientists and their industrial/academic research partners
• ensure that agreements in the MATCH program are consistent with existing agreement and NCI/NIH policy.
• Ad-Hoc Work products and documents related to creating data/monitoring plans and providing regular written reports detailing progress against tasks and milestones
• maintain the “Active Agreements” list on the CTEP Website of current CTEP Agents available for request; maintain the ACG SharePoint Page as requested.

Requirements:

• Master’s degree in Biological Sciences or Life Sciences
• Minimum of three (3) years of experience.

Skills

• Clinical trial project management experience
• Ability to problem solve and prioritize assignments/tasks
• Ability to do work assignments and/or projects successfully and completed in a timely manner
• Familiarity with area of clinical trials preferably in the field of Oncology
• Previous project management experience and/or clinical trial management including data management
• Familiarity with research subcontracting
• Exceptional written and oral communication skills
• Ability to work in a busy setting, both independently and within a team
• Ability to communicate effectively with high-level personnel
• Ability to attend meetings as a program liaison
• Willingness to perform tasks that may fall outside of the normal daily responsibilities
• Ability to obtain and maintain a security clearance

PLEASE APPLY ONLINE

When you apply, please know a Kelly Government Solutions Recruiter will review your resume and will contact you directly, if your skills and experience match the requirements of this position; a full job description can be made available at that time.

Due to the high volume of inquiries, we regret that we cannot accept phone calls. Even if you aren’t contacted for this position, you are still part of our talent network. All Kelly recruiters have access to your profile, which expands your opportunities even further.

As a specialty talent company, Kelly is committed to doing the right thing for our talent and clients.

We stand up for equity, inclusion, fair treatment, and opportunity for all as these build the foundation of our Talent Promise. With a focus on safety, value, well-being, investment, and opportunity, Kelly’s Talent Promise confirms our commitment to those in search of a better way to work and live and to help discover what’s next.

It is obvious things are different than they were just a few months ago. Kelly is at the forefront of ensuring the safety of our employees in this new working environment. Be well and stay strong.

You should know: Vaccination against COVID-19 is a requirement for all job opportunities offered through Kelly Government Solutions, in accordance with the Executive Order on Ensuring Adequate COVID Safety Protocols for Federal Contractors.