Study Lead - Biologics

Location
Kent
Salary
£49000 - £59000 per annum
Posted
30 Mar 2021
Closes
27 Apr 2021
Ref
J5634693
Contact
Christina Giakou
Contract Type
Permanent
Hours
Full Time
We are currently looking for a Study Lead - Biologics to join a leading biopharmaceutical company based in the Canterbury area. As the Study Lead -Biologics you will act as the technical expert and lead any scientific communications with clients on Biopharma CDMO projects. Other responsibilities will include writing scientific reports, presenting to clients and manage relationships.

This is great opportunity for an experienced scientist/ study manager with a strong background in upstream and/or downstream and/or analytical. This is a non-lab based role.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Study Lead - Biologics will be varied however the key duties and responsibilities are as follows:

1. Take the lead role in scientific communications with clients.

2. You will directly support with scientific direction to project teams, assess data and conclusions and specify the preparation of new data where required to meet project objectives.

3. You will act as the Subject Matter Expert within one or more of the below disciplines: Upstream, Downstream or Analytical.

4. You will work closely with the R&D Team Leaders and Director as well as the Business Development Manager and marketing team.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Study Lead - Biologics we are looking to identify the following on your profile and past history:

1. A PhD in Biological Sciences, Life Sciences, Biochemistry, Protein Sciences ets. Post-Doc experience in advantageous.

2. Proven industry experience in cGMP / ISO13485 environment.

3. A strong industry experience in one or more of the following areas: Upstream, Downstream and Analytical.

Key Words: Study Manager / Study Director / Study Lead / Technical Lead / Subject Matter Expert / Upstream / Downstream / Analytical Development / Process Development / GMP / ISO13485

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