Senior Site Contract Manager
at Johnson Johnson
North Ryde, New South Wales, Australia -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 05 Jul, 2024 | Not Specified | 29 Jun, 2024 | 3 year(s) or above | Therapeutic Areas,Contract Negotiation,Clinical Trials | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
- 2024 Best Places to Work – #1 in Health Industry
- Remote role - can be based in Sydney, Melbourne, Brisbane, Perth, or Adelaide
QUALIFICATIONS
- 3 to 5 years-experience and/or equivalent competencies in pharmaceutical industry/clinical research
- Degree in Science, Nursing or Life Sciences
- A strategic mindset with generous competitor awareness
- High-level EQ that facilitates you working well autonomously and as part of a team; and personal commitment to being the best you can be, for our patients, our customers and our company
- Excellent communication and problem-solving skills
- Understanding of the clinical development process
- Highly experienced in contract negotiation for clinical trials across phases 1 to 3 is essentialAbility to work effectively in cross-function teams
Johnson & Johnson, as a world leader across multiple therapy areas, offers a dynamic environment with opportunities to learn and grow across a broad range of those therapeutic areas. We encourage candidates with a strong desire to learn and a willingness to adapt to new challenges to apply.
Responsibilities:
- Prepare, negotiate, and finalize clinical trial agreements for company sponsored
- Participate in discussions related to the development of site/investigator budgets aligned with fair market value
- Manage the contract amendment lifecycle
- Work with the global CCS team as necessary to review and analyse contractual terms to reach resolution
- Work proactively to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites. Mentor and train new contract coordinators and analysts
- Assess risks of budget and legal provisions in conjunction with members of the CCS team and support functions. Escalate any issues as appropriateComply with requests from QA and auditors
REQUIREMENT SUMMARY
Min:3.0Max:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
North Ryde NSW, Australia