Work Schedule
First Shift (Days)
Environmental Conditions
Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse
Job Description
DESCRIPTION:
Join our collaborative team at Thermo Fisher Scientific as a Pharmacist III, where you'll contribute to clinical research and ensure regulatory compliance for investigational drugs and biologics. As part of our Clinical Trials Division, you'll manage pharmaceutical operations, from protocol review to drug distribution, while working with government agencies, manufacturers, and clinical sites worldwide. This position offers the opportunity to impact global health outcomes through oversight of investigational products, quality assurance, and clinical trial support.
REQUIREMENTS:
- Reviews clinical site orders, supports clinical protocols and calculates supply requirements.
- Manages supply levels and expiration date of products, interacting with pharmaceutical manufacturers, communicating with clinical sites, and involvement with packaging and labeling investigation agents.
- Develop and revise SOPs to support operational activities.
- Manage Investigational drug orders.
- Monitor quantity and expiration date of supplies being issued.
- Prepare documents for international shipments and/or apply for FDA import permits.
- Review monitoring reports, pharmacy licensing, notify project Officer of clinical site problems, and maintain database containing a review of all pharmacy contract related items.
- Support proper shipping and distribution of Investigational agents to clinical sites.
- Check and review processed orders.
- Process and investigate any customer complaints or deviations.
- Attend COR meetings and provide updates on study protocol.
- Purchase pharmaceuticals or vaccines to support clinical trials under IND through approved vendors.
- Provide Pharmaceutical costing estimates to COR.
- Provide compounding solutions for future clinical trials.
- Initiate and authorize product recalls.
- Review Certificates of Analysis (CoAs) for clinical agents.
- Establish drug requirements and supply requirements for new protocols.
- Design and create drug labels based on country and regulatory requirements.
- Review protocol revisions for impact on inventory levels and update the COR.
- Research and facilitate purchasing of study products by the networks.
- Develop packaging and labeling requirements to meet US and International packaging and labeling standards.
- Review batch records for accuracy
Education/ Experience:- Requires a Bachelor’s Degree in Pharmacy.
- Requires Maryland Pharmacy License (registered Pharmacist in the State of Maryland).
- Requires 3+ years of experience in the pharmaceutical field.
Certificates and/ or Licenses:Requires Maryland Pharmacy License.
Compensation and Benefits
The salary range estimated for this position based in Maryland is $91,700.00–$137,525.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
