Associate Contracts Manager - FSP

Precision for Medicine

United States

À distance

USD 69 000 - 104 000

Plein temps

Il y a 32 heures
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Avantages offerts par ce poste

Discretionary annual bonus
Health insurance
Retirement savings
Life insurance
Disability benefits
Parental leave
Paid time off

Résumé du poste

Precision Medicine Group is seeking a Contracts Specialist to draft, negotiate, and track clinical research agreements including CDAs, CTAs, and related amendments. The role collaborates with North American and European study teams and sites to ensure timely delivery in line with project timelines.

Responsibilities include managing contract lifecycle, resolving issues with stakeholders, and maintaining documentation in contract databases.

Qualifications

  • 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research (e.g. NDA, CTA).
  • Experience in contract research, life science, biotech or pharmaceutical industry preferred.
  • Experience interacting with European institutions.

Responsabilités

  • Prepare and negotiate CDA, CTA and Amendments, vendor contracts and site budgets.
  • Lead interactions with North American and European study teams and with sites.
  • Coordinate execution of the agreements and maintain contract files and databases.
  • Update study teams and sponsors on contract negotiations and statuses.
  • Ensure adherence to contracting standards and company policies.

Connaissances

Legal contract management
Excellent organizational skills
Strong communication skills
MS Office proficiency
Independent work capability

Formation

Bachelor's degree

Outils

MS Office

Description du poste

Position Summary:

Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosureagreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements(CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations.

Essential functions of the job include but are not limited to:
  • Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendor contracts and site budgets.
  • Lead interactions with the North American and European internal study teams, as applicable
  • Lead interactions regarding the various agreements with the Site(s)
  • Lead interactions regarding assigned agreements with the Sponsor(s)
  • Work with supervisor and various internal/external stakeholders to resolve contractual issues.
  • Ensure adhered to company policies, procedures, and contracting standards.
  • Update relevant study team members and sponsors regarding the status of contractnegotiations and execution.
  • Coordinate execution of the agreements
  • Support the maintenance of contract files and databases, including email anddocument archiving.
  • Other duties as assigned.
Minimum Required:
  • Bachelor’s degree, or equivalent contract management experience preferably in a clinical research or similar industry setting
Other Required:
  • 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as well as management, control and tracking of the contract process.
  • Experience in contract research, life science, biotech or pharmaceutical industry is preferred.
  • Experience interacting with European institutions.
Preferred:
  • Equivalent contract management experience in a clinical research or similar industry setting
  • Experience in contract research, life science, biotech or pharmaceutical industry.
Skills:
Competencies
  • Excellent organizational and communication skills and attention to detail
  • Experience in tracking status for site contracts and budget, filing and distribution.
  • Executes time-sensitive matters while maintaining accuracy and attention to detail.
  • Exhibits high self-motivation and is able to work and plan independently or with limited supervision.
  • Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments and understanding of the service culture and positive interactions with customers.
  • Proficient in MS Office Software programs and computer applications
  • Works well independently and cooperatively with others to achieve common goals in a virtual environment.
  • Develops, maintains and strengthens relationships with others inside or outsideofthe organization who can provide information, assistance and support Mentor and/or Ambassador for new Contract and Budget Associates and PFM staff

Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits.

Reasonable estimate of the current range

$68,700 - $103,700 USD

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com .

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

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