Sr Clinical Research Spec

Planet Pharma; Minneapolis (MN); On-site; USD 62,000 - 76,000; Full time

Job summary

Planet Pharma in Minnesota is seeking a clinician for trials oversight, design, and development of clinical evaluation studies. Responsibilities include protocol creation and patient forms, plus conducting registered and nonregistered studies aligned with medical needs and market potential.

Role involves coordinating with project teams under SOPs and GCP, managing budgets and supply chains; on-site work is preferred with possible remote elements.

Qualifications

• 3+ years of clinical research experience with an in-house sponsor.
• Experience with site activation activities.
• Site management activities.

Responsibilities

• Oversees, designs, plans and develops clinical evaluation research studies; prepares protocols and patient record forms.
• Conducts registered and nonregistered clinical studies of products with medical need or commercial potential.
• Oversees and interprets results of clinical investigations for new drug, device or consumer applications.
• Manages operational aspects of clinical trials with project teams, SOPs, GCP and country regulations; may prepare budgets; may handle clinical supply operations and site/vendor selection.

Skills

Clinical research experience

Site activation

Site management

Education

Bachelor's degree

Job description

Pay 45-55/h depending on experience

HM’s Top Needs:

1. 3 or more years of clinical research experience with in industry sponsor. Preferred med devices.
2. Experience with site activation activities
3. Site management activities

Education Required: Bachelor

Years’ Experience Required:

3 and more

Will the contractor be working 40 hours a week? If not, weekly estimate?

Ideally 40h/week

Work Location:

Do they need to be local to any MDT office and if so where?

Preferably on-site in Minnesota office (alternatives could be Colorado and Irvine, but let’s look for Minnesota first)

Yes, given the option to convert to NV employee for which in-office will be required.

Responsibilities may include the following and other duties may be assigned. Oversees, designs, plans and develops clinical evaluation research studies. Prepares and authors protocols and patient record forms. Conducts registered and nonregistered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential. Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application. Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets. May be responsible for clinical supply operations, site and vendor selection.

SPECIALIST CAREER STREAM:

Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University).

DIFFERENTIATING FACTORS

Autonomy: Seasoned individual contributor. Works independently under limited supervision to determine and develop approach to solutions. Coaches and reviews the work of lower level specialists; may manage projects / processes.

Organizational Impact: May be responsible for entire projects or processes within job area. Contributes to the completion of work group objectives, through building relationships and consensus to reach agreements on assignments.

Innovation and Complexity: Problems and issues faced are difficult, and may require understanding of multiple issues, job areas or specialties . Makes improvements of processes, systems or products to enhance performance of the job area. Analysis provided is indepth in nature and often provides recommendations on process improvements.

Communication and Influence: Communicates with senior internal and external customers and vendors. Exchange information of facts, statuses, ideas and issues to achieve objective, and influence decisionmaking.

Leadership and Talent Management: May provide guidance, coaching and training to other employees within job area. May manage projects, requiring delegation of work and review of others’ work product .

Required Knowledge and Experience: Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience. May have practical knowledge of project management. Requires a University Degree and minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.